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ICD-10
HPO
Compare GWAS
Super Class
Top
Sub Class
Nutritional anaemias
Haemolytic anaemias
Aplastic and other anaemias
Coagulation defects, purpura and other haemorrhagic conditions
Other diseases of blood and blood-forming organs
Certain disorders involving the immune mechanism
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Chapter3
Case/Control GWAS
ⓘ
Links
Sex Split
Interactive Plot
Statistics
Case
Control
34091
426115
Top SNP Information
Show Table
Location
SNP
Gene
Ref>Alt
Alt in Case
Alt in Control
Chi-square
P-value
Odds Ratio
chr8:145639681
rs1871534
SLC39A4
G>C
2469
15676
936.6
1.111e-205
1.937
chr1:159174683
rs2814778
ACKR1
T>C
2598
16779
933.8
4.467e-205
1.904
chr19:42393286
rs717225
ARHGEF1
A>G
2744
19199
754.9
3.402e-166
1.757
chr15:45556163
rs8023604
SLC28A2
T>C
1794
11117
727.0
4.004e-160
1.976
chr1:207782889
rs17047661
CR1
A>G
1935
12384
712.2
6.779e-157
1.914
chr5:33951693
rs16891982
SLC45A2
G>C
6891
60170
712.1
7.013e-157
1.425
chr3:188327555
rs7645635
LPP
T>C
1930
12446
693.1
9.664e-153
1.899
chr8:10557760
rs57041981
RP1L1
A>G
2164
14484
691.4
2.237e-152
1.832
chr17:58508582
rs8071181
C17orf64
G>A
2033
13384
683.3
1.291e-150
1.86
chr19:42392441
rs16975619
ARHGEF1
T>C
2496
17514
679.1
1.073e-149
1.75
chr6:136480972
rs9483910
PDE7B
C>T
2631
18741
675.8
5.598e-149
1.723
chr17:29350769
rs8073072
-
T>G
3053
22653
674.1
1.279e-148
1.658
chr17:29290106
rs55861543
-
C>T
2561
18198
665.5
9.3e-147
1.728
chr9:117110112
Affx-52344420
AKNA
T>TG
1931
12648
661.0
8.868e-146
1.87
chr2:66725070
rs12995572
MEIS1
G>C
3182
23969
660.4
1.22e-145
1.633
chr15:48426484
rs1426654
SLC24A5
A>G
3213
24313
655.1
1.758e-144
1.626
chr1:173579034
rs12065033
AL139142.2
C>T
2005
13336
653.1
4.762e-144
1.842
chr18:9536315
rs14336
RALBP1
A>C
1743
11124
646.0
1.668e-142
1.917
chr12:132549300
rs7136109
EP400
A>G
1498
9132
635.5
3.104e-140
2.005
chr19:42391425
rs28521795
ARHGEF1
G>A
2342
16480
629.1
7.928e-139
1.743
chr6:32603007
rs2040406
HLA-DQA1
A>G
12976
148480
112.7
2.467e-26
1.114
chr6:32659645
rs2856674
-
A>G
10921
123941
108.0
2.712e-25
1.12
chr6:32657436
rs3129716
-
T>C
10845
123384
103.9
2.123e-24
1.118
chr6:32605884
rs2187668
HLA-DQA1
C>T
10668
121453
102.7
3.816e-24
1.118
chr6:32626272
rs9273363
-
C>A
21657
254955
102.4
4.469e-24
1.09
chr6:32626302
rs9273364
-
T>G
21093
248415
100.6
1.129e-23
1.091
chr6:32290208
rs9268235
TSBP1
C>T
9750
110745
94.56
2.374e-22
1.117
chr6:32345689
rs2894254
-
T>G
9586
108990
89.97
2.423e-21
1.115
chr6:32666526
rs1794282
-
C>T
9483
107796
89.96
2.433e-21
1.116
chr6:32261252
rs7775397
TSBP1
T>G
9622
109502
89.23
3.517e-21
1.114
chr6:32333827
rs3129927
TSBP1
A>C
9624
109527
89.12
3.715e-21
1.114
chr6:32623150
rs3021302
-
T>C
12177
140347
89.09
3.764e-21
1.103
chr6:32325562
rs2395149
TSBP1
G>A
9610
109444
88.38
5.41e-21
1.114
chr6:32303692
rs1265754
TSBP1
T>A
9622
109577
88.29
5.642e-21
1.114
chr6:32080191
rs1269852
TNXB
G>C
9621
109574
87.85
7.056e-21
1.113
chr6:32310863
rs2849018
TSBP1
T>C
9616
109576
86.66
1.286e-20
1.113
chr6:32302382
rs1265757
TSBP1
C>T
9590
109313
86.58
1.342e-20
1.113
chr6:32408497
rs3135394
HLA-DRA
A>G
9567
109069
86.2
1.624e-20
1.113
chr6:32395726
rs3129843
-
A>G
9545
108777
86.12
1.692e-20
1.113
chr6:32765585
rs9276731
-
G>T
8951
101656
86.04
1.763e-20
1.116
Associated Phenotypes
ⓘ
Shared SNP phenotypes
No shared SNP phenotypes
ID
Name
Top Correlation
HP: 0000008
Abnormal morphology of female internal genitalia
10/20
HP: 0000032
Abnormality of male external genitalia
2/20
HP: 0000055
Abnormality of female external genitalia
1/20
HP: 0000058
Abnormality of the labia
1/20
HP: 0000066
Labial hypoplasia
1/20
HP: 0000075
Renal duplication
1/20
HP: 0000077
Abnormality of the kidney
7/20
HP: 0000078
Abnormality of the genital system
3/20
HP: 0000079
Abnormality of the urinary system
6/20
HP: 0000095
Abnormality of renal glomerulus morphology
2/20
HP: 0000118
Phenotypic abnormality
2/20
HP: 0000119
Abnormality of the genitourinary system
5/20
HP: 0000123
Nephritis
4/20
HP: 0000132
Menorrhagia
13/20
HP: 0000140
Abnormality of the menstrual cycle
14/20
HP: 0000152
Abnormality of head or neck
1/20
HP: 0000157
Abnormality of the tongue
2/20
HP: 0000159
Abnormal lip morphology
2/20
HP: 0000164
Abnormality of the dentition
11/20
HP: 0000168
Abnormality of the gingiva
7/20
HP: 0000234
Abnormality of the head
1/20
HP: 0000277
Abnormality of the mandible
7/20
HP: 0000282
Facial edema
4/20
HP: 0000356
Abnormality of the outer ear
6/20
HP: 0000357
Abnormal location of ears
1/20
HP: 0000359
Abnormality of the inner ear
2/20
HP: 0000479
Abnormal retinal morphology
12/20
HP: 0000492
Abnormal eyelid morphology
2/20
HP: 0000573
Retinal hemorrhage
11/20
HP: 0000598
Abnormality of the ear
5/20
HP: 0000606
Abnormality of the periorbital region
4/20
HP: 0000707
Abnormality of the nervous system
1/20
HP: 0000736
Short attention span
3/20
HP: 0000752
Hyperactivity
3/20
HP: 0000765
Abnormality of the thorax
1/20
HP: 0000811
Abnormal external genitalia
2/20
HP: 0000812
Abnormal internal genitalia
8/20
HP: 0000828
Abnormality of the parathyroid gland
8/20
HP: 0000858
Irregular menstruation
14/20
HP: 0000860
Parathyroid hypoplasia
11/20
HP: 0000864
Abnormality of the hypothalamus-pituitary axis
5/20
HP: 0000924
Abnormality of the skeletal system
1/20
HP: 0000929
Abnormal skull morphology
1/20
HP: 0000953
Hyperpigmentation of the skin
5/20
HP: 0000961
Cyanosis
1/20
HP: 0000964
Eczema
5/20
HP: 0000973
Cutis laxa
1/20
HP: 0000979
Purpura
1/20
HP: 0001000
Abnormality of skin pigmentation
8/20
HP: 0001010
Hypopigmentation of the skin
8/20
HP: 0001025
Urticaria
5/20
HP: 0001028
Hemangioma
1/20
HP: 0001051
Seborrheic dermatitis
2/20
HP: 0001067
Neurofibromas
1/20
HP: 0001098
Abnormal fundus morphology
1/20
HP: 0001155
Abnormality of the hand
6/20
HP: 0001159
Syndactyly
4/20
HP: 0001167
Abnormality of finger
5/20
HP: 0001172
Abnormal thumb morphology
8/20
HP: 0001197
Abnormality of prenatal development or birth
13/20
HP: 0001367
Abnormal joint morphology
2/20
HP: 0001369
Arthritis
2/20
HP: 0001397
Hepatic steatosis
5/20
HP: 0001438
Abnormality of abdomen morphology
1/20
HP: 0001510
Growth delay
5/20
HP: 0001518
Small for gestational age
9/20
HP: 0001595
Abnormal hair morphology
6/20
HP: 0001608
Abnormality of the voice
1/20
HP: 0001626
Abnormality of the cardiovascular system
1/20
HP: 0001645
Sudden cardiac death
2/20
HP: 0001678
Atrioventricular block
4/20
HP: 0001679
Abnormal aortic morphology
5/20
HP: 0001695
Cardiac arrest
4/20
HP: 0001746
Asplenia
1/20
HP: 0001760
Abnormality of the foot
3/20
HP: 0001770
Toe syndactyly
5/20
HP: 0001780
Abnormality of toe
4/20
HP: 0001844
Abnormality of the hallux
7/20
HP: 0001871
Abnormality of blood and blood-forming tissues
2/20
HP: 0001872
Abnormal thrombocyte morphology
2/20
HP: 0001873
Thrombocytopenia
2/20
HP: 0001876
Pancytopenia
2/20
HP: 0001877
Abnormal erythrocyte morphology
16/20
HP: 0001878
Hemolytic anemia
15/20
HP: 0001881
Abnormal leukocyte morphology
2/20
HP: 0001888
Lymphopenia
1/20
HP: 0001889
Megaloblastic anemia
4/20
HP: 0001890
Autoimmune hemolytic anemia
14/20
HP: 0001891
Iron deficiency anemia
9/20
HP: 0001892
Abnormal bleeding
5/20
HP: 0001896
Reticulocytopenia
4/20
HP: 0001903
Anemia
15/20
HP: 0001908
Hypoplastic anemia
1/20
HP: 0001909
Leukemia
1/20
HP: 0001915
Aplastic anemia
2/20
HP: 0001930
Nonspherocytic hemolytic anemia
2/20
HP: 0001931
Hypochromic anemia
9/20
HP: 0001935
Microcytic anemia
6/20
HP: 0001939
Abnormality of metabolism/homeostasis
5/20
HP: 0001943
Hypoglycemia
7/20
HP: 0001944
Dehydration
3/20
HP: 0001945
Fever
6/20
HP: 0001965
Abnormality of the scalp
3/20
HP: 0001972
Macrocytic anemia
5/20
HP: 0001977
Abnormal thrombosis
2/20
HP: 0001980
Megaloblastic bone marrow
7/20
HP: 0001986
Hypertonic dehydration
3/20
HP: 0001988
Recurrent hypoglycemia
3/20
HP: 0001999
Abnormal facial shape
3/20
HP: 0002011
Morphological central nervous system abnormality
2/20
HP: 0002013
Vomiting
7/20
HP: 0002014
Diarrhea
8/20
HP: 0002017
Nausea and vomiting
7/20
HP: 0002031
Abnormal esophagus morphology
5/20
HP: 0002034
Abnormality of the rectum
9/20
HP: 0002046
Heat intolerance
1/20
HP: 0002086
Abnormality of the respiratory system
1/20
HP: 0002087
Abnormality of the upper respiratory tract
2/20
HP: 0002088
Abnormal lung morphology
1/20
HP: 0002094
Dyspnea
1/20
HP: 0002098
Respiratory distress
1/20
HP: 0002205
Recurrent respiratory infections
6/20
HP: 0002239
Gastrointestinal hemorrhage
9/20
HP: 0002240
Hepatomegaly
1/20
HP: 0002242
Abnormal intestine morphology
2/20
HP: 0002250
Abnormal large intestine morphology
6/20
HP: 0002293
Alopecia of scalp
2/20
HP: 0002304
Akinesia
1/20
HP: 0002488
Acute leukemia
1/20
HP: 0002572
Episodic vomiting
4/20
HP: 0002585
Abnormality of the peritoneum
1/20
HP: 0002597
Abnormality of the vasculature
1/20
HP: 0002664
Neoplasm
2/20
HP: 0002686
Prenatal maternal abnormality
12/20
HP: 0002715
Abnormality of the immune system
1/20
HP: 0002716
Lymphadenopathy
6/20
HP: 0002718
Recurrent bacterial infections
1/20
HP: 0002721
Immunodeficiency
8/20
HP: 0002730
Chronic noninfectious lymphadenopathy
2/20
HP: 0002731
Decreased lymphocyte apoptosis
2/20
HP: 0002733
Abnormality of the lymph nodes
4/20
HP: 0002754
Osteomyelitis
9/20
HP: 0002813
Abnormality of limb bone morphology
2/20
HP: 0002814
Abnormality of the lower limb
2/20
HP: 0002817
Abnormality of the upper limb
3/20
HP: 0002843
Abnormal T cell morphology
8/20
HP: 0002863
Myelodysplasia
9/20
HP: 0002955
Granulomatosis
7/20
HP: 0002960
Autoimmunity
10/20
HP: 0002963
Abnormal delayed hypersensitivity skin test
5/20
HP: 0002965
Cutaneous anergy
5/20
HP: 0003010
Prolonged bleeding time
8/20
HP: 0003011
Abnormality of the musculature
1/20
HP: 0003040
Arthropathy
4/20
HP: 0003072
Hypercalcemia
1/20
HP: 0003110
Abnormality of urine homeostasis
11/20
HP: 0003112
Abnormality of serum amino acid level
11/20
HP: 0003155
Elevated alkaline phosphatase
10/20
HP: 0003158
Hyposthenuria
14/20
HP: 0003201
Rhabdomyolysis
12/20
HP: 0003237
Increased circulating IgG level
4/20
HP: 0003241
External genital hypoplasia
1/20
HP: 0003330
Abnormal bone structure
1/20
HP: 0003422
Vertebral segmentation defect
7/20
HP: 0003496
Increased circulating IgM level
3/20
HP: 0003549
Abnormality of connective tissue
7/20
HP: 0004296
Abnormality of gastrointestinal vasculature
4/20
HP: 0004311
Abnormal macrophage morphology
6/20
HP: 0004312
Abnormal reticulocyte morphology
5/20
HP: 0004327
Abnormal vitreous humor morphology
4/20
HP: 0004329
Abnormal posterior eye segment morphology
6/20
HP: 0004332
Abnormal lymphocyte morphology
2/20
HP: 0004340
Abnormality of vitamin B metabolism
7/20
HP: 0004341
Abnormality of vitamin B12 metabolism
7/20
HP: 0004354
Abnormal circulating carboxylic acid concentration
13/20
HP: 0004364
Abnormal circulating nitrogen compound concentration
7/20
HP: 0004370
Abnormality of temperature regulation
8/20
HP: 0004372
Reduced consciousness/confusion
2/20
HP: 0004375
Neoplasm of the nervous system
1/20
HP: 0004377
Hematological neoplasm
9/20
HP: 0004379
Abnormality of alkaline phosphatase activity
10/20
HP: 0004431
Complement deficiency
8/20
HP: 0004433
Secretory IgA deficiency
5/20
HP: 0004444
Spherocytosis
4/20
HP: 0004445
Elliptocytosis
13/20
HP: 0004447
Poikilocytosis
16/20
HP: 0004552
Scarring alopecia of scalp
2/20
HP: 0004802
Episodic hemolytic anemia
11/20
HP: 0004804
Congenital hemolytic anemia
2/20
HP: 0004809
Neonatal alloimmune thrombocytopenia
8/20
HP: 0004840
Hypochromic microcytic anemia
8/20
HP: 0004859
Amegakaryocytic thrombocytopenia
9/20
HP: 0004870
Chronic hemolytic anemia
8/20
HP: 0004905
Low levels of vitamin A
1/20
HP: 0004906
Hypernatremic dehydration
3/20
HP: 0005105
Abnormal nasal morphology
7/20
HP: 0005150
Abnormal atrioventricular conduction
4/20
HP: 0005224
Rectal abscess
2/20
HP: 0005261
Joint hemorrhage
2/20
HP: 0005262
Abnormality of the synovia
4/20
HP: 0005339
Abnormality of complement system
11/20
HP: 0005344
Abnormal carotid artery morphology
4/20
HP: 0005403
Decrease in T cell count
4/20
HP: 0005421
Decreased serum complement C3
5/20
HP: 0005505
Refractory anemia
3/20
HP: 0005507
Hemoglobin Barts
16/20
HP: 0005528
Bone marrow hypocellularity
10/20
HP: 0005558
Chronic leukemia
2/20
HP: 0005561
Abnormality of bone marrow cell morphology
2/20
HP: 0005607
Abnormal tracheobronchial morphology
2/20
HP: 0005622
Broad long bones
10/20
HP: 0005918
Abnormal finger phalanx morphology
5/20
HP: 0005922
Abnormal hand morphology
7/20
HP: 0006009
Broad phalanx
10/20
HP: 0006101
Finger syndactyly
4/20
HP: 0006261
Abnormal phalangeal joint morphology of the hand
4/20
HP: 0006292
Abnormality of dental eruption
7/20
HP: 0006335
Persistence of primary teeth
7/20
HP: 0006482
Abnormality of dental morphology
10/20
HP: 0006493
Aplasia/hypoplasia involving bones of the lower limbs
3/20
HP: 0006494
Aplasia/Hypoplasia involving bones of the feet
8/20
HP: 0006516
Hypersensitivity pneumonitis
4/20
HP: 0006533
Bronchodysplasia
14/20
HP: 0006561
Lipid accumulation in hepatocytes
5/20
HP: 0006562
Viral hepatitis
8/20
HP: 0006573
Acute hepatic steatosis
8/20
HP: 0006824
Cranial nerve paralysis
1/20
HP: 0007018
Attention deficit hyperactivity disorder
3/20
HP: 0007274
Recurrent bacterial meningitis
1/20
HP: 0007626
Mandibular osteomyelitis
10/20
HP: 0008046
Abnormal retinal vascular morphology
2/20
HP: 0008047
Abnormality of the vasculature of the eye
5/20
HP: 0008067
Abnormally lax or hyperextensible skin
2/20
HP: 0008069
Neoplasm of the skin
3/20
HP: 0008372
Abnormality of vitamin A metabolism
1/20
HP: 0008373
Puberty and gonadal disorders
13/20
HP: 0009045
Exercise-induced rhabdomyolysis
13/20
HP: 0009115
Aplasia/hypoplasia involving the skeleton
2/20
HP: 0009815
Aplasia/hypoplasia of the extremities
2/20
HP: 0009817
Aplasia involving bones of the lower limbs
1/20
HP: 0009825
Aplasia involving bones of the extremities
1/20
HP: 0009887
Abnormality of hair pigmentation
8/20
HP: 0010451
Aplasia/Hypoplasia of the spleen
1/20
HP: 0010460
Abnormality of the female genitalia
5/20
HP: 0010461
Abnormality of the male genitalia
2/20
HP: 0010614
Fibroma
2/20
HP: 0010621
Cutaneous syndactyly of toes
5/20
HP: 0010628
Facial palsy
1/20
HP: 0010702
Increased antibody level in blood
6/20
HP: 0010720
Abnormal hair pattern
7/20
HP: 0010732
Nodular changes affecting the eyelids
3/20
HP: 0010766
Ectopic calcification
7/20
HP: 0010827
Abnormality of the seventh cranial nerve
1/20
HP: 0010935
Abnormality of the upper urinary tract
7/20
HP: 0010937
Abnormality of the nasal skeleton
7/20
HP: 0010939
Abnormality of the nasal bone
7/20
HP: 0010972
Anemia of inadequate production
10/20
HP: 0010978
Abnormality of immune system physiology
1/20
HP: 0010987
Abnormal cellular immune system morphology
2/20
HP: 0011004
Abnormal systemic arterial morphology
4/20
HP: 0011014
Abnormal glucose homeostasis
6/20
HP: 0011015
Abnormal blood glucose concentration
11/20
HP: 0011024
Abnormality of the gastrointestinal tract
4/20
HP: 0011025
Abnormal cardiovascular system physiology
1/20
HP: 0011028
Abnormality of blood circulation
2/20
HP: 0011029
Internal hemorrhage
2/20
HP: 0011035
Abnormal renal cortex morphology
2/20
HP: 0011061
Abnormality of dental structure
12/20
HP: 0011077
Abnormality of molar
2/20
HP: 0011121
Abnormality of skin morphology
2/20
HP: 0011122
Abnormality of skin physiology
5/20
HP: 0011123
Inflammatory abnormality of the skin
4/20
HP: 0011138
Abnormality of skin adnexa morphology
5/20
HP: 0011276
Vascular skin abnormality
2/20
HP: 0011277
Abnormality of the urinary system physiology
7/20
HP: 0011297
Abnormal digit morphology
4/20
HP: 0011314
Abnormality of long bone morphology
1/20
HP: 0011354
Generalized abnormality of skin
1/20
HP: 0011355
Localized skin lesion
4/20
HP: 0011360
Acquired abnormal hair pattern
5/20
HP: 0011531
Vitritis
8/20
HP: 0011675
Arrhythmia
1/20
HP: 0011729
Abnormality of joint mobility
4/20
HP: 0011747
Abnormality of the anterior pituitary
7/20
HP: 0011766
Abnormality of the parathyroid morphology
6/20
HP: 0011768
Parathyroid dysgenesis
8/20
HP: 0011792
Neoplasm by histology
3/20
HP: 0011793
Neoplasm by anatomical site
2/20
HP: 0011799
Abnormality of facial soft tissue
3/20
HP: 0011804
Abnormal muscle physiology
4/20
HP: 0011805
Abnormal skeletal muscle morphology
1/20
HP: 0011839
Abnormal T cell count
8/20
HP: 0011840
Abnormality of T cell physiology
3/20
HP: 0011842
Abnormality of skeletal morphology
1/20
HP: 0011844
Abnormal appendicular skeleton morphology
2/20
HP: 0011873
Abnormal platelet count
2/20
HP: 0011885
Hemorrhage of the eye
13/20
HP: 0011890
Prolonged bleeding following procedure
10/20
HP: 0011891
Post-partum hemorrhage
9/20
HP: 0011893
Abnormal leukocyte count
2/20
HP: 0011895
Anemia due to reduced life span of red cells
15/20
HP: 0011899
Hyperfibrinogenemia
2/20
HP: 0011900
Hypofibrinogenemia
1/20
HP: 0011902
Abnormal hemoglobin
15/20
HP: 0011903
HbH hemoglobin
8/20
HP: 0012086
Abnormal urinary color
10/20
HP: 0012115
Hepatitis
11/20
HP: 0012124
Intermediate uveitis
9/20
HP: 0012130
Abnormal erythroid lineage cell morphology
16/20
HP: 0012145
Abnormality of multiple cell lineages in the bone marrow
2/20
HP: 0012174
Glioblastoma multiforme
1/20
HP: 0012209
Juvenile myelomonocytic leukemia
4/20
HP: 0012210
Abnormal renal morphology
1/20
HP: 0012211
Abnormal renal physiology
8/20
HP: 0012219
Erythema nodosum
7/20
HP: 0012243
Abnormal reproductive system morphology
4/20
HP: 0012252
Abnormal respiratory system morphology
1/20
HP: 0012303
Abnormal aortic arch morphology
1/20
HP: 0012324
Myeloid leukemia
3/20
HP: 0012335
Abnormality of folate metabolism
6/20
HP: 0012337
Abnormal homeostasis
4/20
HP: 0012343
Decreased serum ferritin
1/20
HP: 0012379
Abnormal enzyme/coenzyme activity
10/20
HP: 0012415
Abnormal blood gas level
3/20
HP: 0012443
Abnormality of brain morphology
2/20
HP: 0012503
Abnormality of the pituitary gland
5/20
HP: 0012531
Pain
1/20
HP: 0012639
Abnormal nervous system morphology
1/20
HP: 0012647
Abnormal inflammatory response
1/20
HP: 0012649
Increased inflammatory response
1/20
HP: 0012718
Morphological abnormality of the gastrointestinal tract
2/20
HP: 0012719
Functional abnormality of the gastrointestinal tract
4/20
HP: 0012722
Heart block
3/20
HP: 0012725
Cutaneous syndactyly
4/20
HP: 0012732
Anorectal anomaly
7/20
HP: 0012735
Cough
1/20
HP: 0012815
Hypoplastic female external genitalia
1/20
HP: 0020047
Abnormal myeloid cell morphology
16/20
HP: 0020085
Infection following live vaccination
2/20
HP: 0020087
BCGosis
2/20
HP: 0020122
Bite cells
1/20
HP: 0025015
Abnormal vascular morphology
8/20
HP: 0025032
Abnormality of digestive system physiology
1/20
HP: 0025059
Splenic abscess
5/20
HP: 0025060
Multifocal splenic abscess
2/20
HP: 0025061
Unifocal splenic abscess
4/20
HP: 0025065
Abnormal mean corpuscular volume
6/20
HP: 0025066
Decreased mean corpuscular volume
6/20
HP: 0025085
Bloody diarrhea
8/20
HP: 0025131
Finger swelling
1/20
HP: 0025142
Constitutional symptom
1/20
HP: 0025270
Abnormality of esophagus physiology
5/20
HP: 0025343
Lupus anticoagulant
10/20
HP: 0025426
Abnormal bronchus morphology
2/20
HP: 0025461
Abnormal cell morphology
10/20
HP: 0025473
Hyperpigmented papule
7/20
HP: 0025546
Abnormal mean corpuscular hemoglobin concentration
14/20
HP: 0025548
Increased mean corpuscular hemoglobin concentration
14/20
HP: 0030058
Sickled erythrocytes
14/20
HP: 0030150
Plasmacytosis
6/20
HP: 0030250
Pulmonary granulomatosis
7/20
HP: 0030319
Weakness of facial musculature
5/20
HP: 0030423
Splenic cyst
1/20
HP: 0030448
Soft tissue sarcoma
13/20
HP: 0030791
Abnormal jaw morphology
3/20
HP: 0030831
Rhonchi
6/20
HP: 0030886
Abnormal lymphocyte apoptosis
2/20
HP: 0030956
Abnormality of cardiovascular system electrophysiology
1/20
HP: 0030962
Abnormal morphology of the great vessels
1/20
HP: 0030972
Abnormal systemic blood pressure
7/20
HP: 0030976
Abnormal factor VIII activity
1/20
HP: 0031137
Storage in hepatocytes
5/20
HP: 0031246
Nonproductive cough
1/20
HP: 0031263
Abnormal renal corpuscle morphology
2/20
HP: 0031363
Palpable purpura
1/20
HP: 0031546
Cardiac conduction abnormality
3/20
HP: 0031611
Sub-inner limiting membrane hemorrhage
12/20
HP: 0031690
Opportunistic infection
1/20
HP: 0031703
Abnormal ear morphology
6/20
HP: 0031803
Fundus hemorrhage
11/20
HP: 0031811
Bilirubinuria
12/20
HP: 0031904
Abnormal total hemolytic complement activity
9/20
HP: 0031950
Usual interstitial pneumonia
1/20
HP: 0032146
HbC hemoglobin
15/20
HP: 0032147
Erythromelalgia
2/20
HP: 0032180
Abnormal circulating metabolite concentration
6/20
HP: 0032220
Interface hepatitis
2/20
HP: 0032231
Hypochromia
8/20
HP: 0032245
Abnormal metabolism
14/20
HP: 0032251
Abnormal immune system morphology
1/20
HP: 0032252
Granuloma
8/20
HP: 0032256
Histoplasmosis
1/20
HP: 0032263
Increased blood pressure
8/20
HP: 0032367
Abnormal growth hormone level
1/20
HP: 0040064
Abnormality of limbs
2/20
HP: 0040068
Abnormality of limb bone
2/20
HP: 0040069
Abnormal lower limb bone morphology
4/20
HP: 0040070
Abnormal upper limb bone morphology
2/20
HP: 0040087
Abnormal blood folate concentration
6/20
HP: 0040126
Abnormal vitamin B12 level
2/20
HP: 0045042
Decreased serum complement C4
9/20
HP: 0045043
Decreased serum complement C4a
9/20
HP: 0045047
HbS hemoglobin
14/20
HP: 0045048
Increased HbA2 hemoglobin
15/20
HP: 0045060
Aplasia/hypoplasia involving bones of the extremities
2/20
HP: 0100006
Neoplasm of the central nervous system
2/20
HP: 0100022
Abnormality of movement
1/20
HP: 0100037
Abnormality of the scalp hair
6/20
HP: 0100240
Synostosis of joints
4/20
HP: 0100242
Sarcoma
13/20
HP: 0100313
Cerebral granulomatosis
8/20
HP: 0100502
Vitamin B12 deficiency
2/20
HP: 0100507
Reduced blood folate concentration
6/20
HP: 0100508
Abnormality of vitamin metabolism
8/20
HP: 0100536
Abnormality of the fascia
3/20
HP: 0100537
Fasciitis
3/20
HP: 0100539
Periorbital edema
4/20
HP: 0100699
Scarring
1/20
HP: 0100705
Abnormality of the glial cells
6/20
HP: 0100721
Mediastinal lymphadenopathy
5/20
HP: 0100742
Vascular neoplasm
1/20
HP: 0100763
Abnormality of the lymphatic system
2/20
HP: 0100778
Cryoglobulinemia
4/20
HP: 0100825
Cheilitis
1/20
HP: 0100872
Abnormality of the plantar skin of foot
6/20
HP: 0200023
Priapism
8/20
HP: 0200036
Skin nodule
2/20
HP: 0200058
Angiosarcoma
1/20
HP: 0410000
Abnormality of vomer
6/20
HP: 0410134
Physical urticaria
6/20
HP: 0410135
Cold urticaria
9/20
HP: 0410242
Abnormal IgG level
4/20
HP: 0410243
Abnormal IgM level
3/20
ID
Name
Top Correlation
HP: 0000002
Abnormality of body height
0/20
HP: 0000036
Abnormality of the penis
0/20
HP: 0000064
Hypoplastic labia minora
0/20
HP: 0000099
Glomerulonephritis
0/20
HP: 0000121
Nephrocalcinosis
0/20
HP: 0000153
Abnormality of the mouth
0/20
HP: 0000163
Abnormal oral cavity morphology
0/20
HP: 0000206
Glossitis
0/20
HP: 0000221
Furrowed tongue
0/20
HP: 0000225
Gingival bleeding
0/20
HP: 0000245
Abnormality of the paranasal sinuses
0/20
HP: 0000246
Sinusitis
0/20
HP: 0000271
Abnormality of the face
0/20
HP: 0000301
Abnormality of facial musculature
0/20
HP: 0000315
Abnormality of the orbital region
0/20
HP: 0000358
Posteriorly rotated ears
0/20
HP: 0000366
Abnormality of the nose
0/20
HP: 0000368
Low-set, posteriorly rotated ears
0/20
HP: 0000369
Low-set ears
0/20
HP: 0000471
Gastrointestinal angiodysplasia
0/20
HP: 0000478
Abnormality of the eye
0/20
HP: 0000553
Abnormal uvea morphology
0/20
HP: 0000554
Uveitis
0/20
HP: 0000630
Abnormal retinal artery morphology
0/20
HP: 0000676
Abnormality of the incisor
0/20
HP: 0000682
Abnormality of dental enamel
0/20
HP: 0000691
Microdontia
0/20
HP: 0000708
Behavioral abnormality
0/20
HP: 0000716
Depressivity
0/20
HP: 0000759
Abnormal peripheral nervous system morphology
0/20
HP: 0000766
Abnormality of the sternum
0/20
HP: 0000777
Abnormality of the thymus
0/20
HP: 0000778
Hypoplasia of the thymus
0/20
HP: 0000793
Membranoproliferative glomerulonephritis
0/20
HP: 0000830
Anterior hypopituitarism
0/20
HP: 0000925
Abnormality of the vertebral column
0/20
HP: 0000951
Abnormality of the skin
0/20
HP: 0000969
Edema
0/20
HP: 0000976
Eczematoid dermatitis
0/20
HP: 0000980
Pallor
0/20
HP: 0000987
Atypical scarring of skin
0/20
HP: 0000991
Xanthomatosis
0/20
HP: 0001005
Dermatological manifestations of systemic disorders
0/20
HP: 0001032
Absent distal interphalangeal creases
0/20
HP: 0001114
Xanthelasma
0/20
HP: 0001254
Lethargy
0/20
HP: 0001291
Abnormal cranial nerve morphology
0/20
HP: 0001324
Muscle weakness
0/20
HP: 0001392
Abnormality of the liver
0/20
HP: 0001409
Portal hypertension
0/20
HP: 0001433
Hepatosplenomegaly
0/20
HP: 0001482
Subcutaneous nodule
0/20
HP: 0001507
Growth abnormality
0/20
HP: 0001541
Ascites
0/20
HP: 0001574
Abnormality of the integument
0/20
HP: 0001581
Recurrent skin infections
0/20
HP: 0001593
Maxillary lateral incisor microdontia
0/20
HP: 0001596
Alopecia
0/20
HP: 0001597
Abnormality of the nail
0/20
HP: 0001709
Third degree atrioventricular block
0/20
HP: 0001743
Abnormality of the spleen
0/20
HP: 0001744
Splenomegaly
0/20
HP: 0001747
Accessory spleen
0/20
HP: 0001748
Polysplenia
0/20
HP: 0001789
Hydrops fetalis
0/20
HP: 0001791
Fetal ascites
0/20
HP: 0001874
Abnormality of neutrophils
0/20
HP: 0001875
Neutropenia
0/20
HP: 0001879
Abnormal eosinophil morphology
0/20
HP: 0001880
Eosinophilia
0/20
HP: 0001882
Leukopenia
0/20
HP: 0001894
Thrombocytosis
0/20
HP: 0001895
Normochromic anemia
0/20
HP: 0001898
Increased red blood cell mass
0/20
HP: 0001900
Increased hemoglobin
0/20
HP: 0001901
Polycythemia
0/20
HP: 0001905
Congenital thrombocytopenia
0/20
HP: 0001911
Abnormal granulocyte morphology
0/20
HP: 0001913
Granulocytopenia
0/20
HP: 0001923
Reticulocytosis
0/20
HP: 0001924
Sideroblastic anemia
0/20
HP: 0001928
Abnormality of coagulation
0/20
HP: 0001929
Reduced factor XI activity
0/20
HP: 0001933
Subcutaneous hemorrhage
0/20
HP: 0001937
Microangiopathic hemolytic anemia
0/20
HP: 0001959
Polydipsia
0/20
HP: 0001971
Hypersplenism
0/20
HP: 0001973
Autoimmune thrombocytopenia
0/20
HP: 0001974
Leukocytosis
0/20
HP: 0001978
Extramedullary hematopoiesis
0/20
HP: 0002012
Abnormality of the abdominal organs
0/20
HP: 0002015
Dysphagia
0/20
HP: 0002023
Anal atresia
0/20
HP: 0002033
Poor suck
0/20
HP: 0002039
Anorexia
0/20
HP: 0002060
Abnormal cerebral morphology
0/20
HP: 0002113
Pulmonary infiltrates
0/20
HP: 0002157
Azotemia
0/20
HP: 0002164
Nail dysplasia
0/20
HP: 0002206
Pulmonary fibrosis
0/20
HP: 0002249
Melena
0/20
HP: 0002269
Abnormality of neuronal migration
0/20
HP: 0002282
Gray matter heterotopia
0/20
HP: 0002292
Frontal balding
0/20
HP: 0002374
Diminished movement
0/20
HP: 0002514
Cerebral calcification
0/20
HP: 0002577
Abnormality of the stomach
0/20
HP: 0002579
Gastrointestinal dysmotility
0/20
HP: 0002586
Peritonitis
0/20
HP: 0002590
Paralytic ileus
0/20
HP: 0002595
Ileus
0/20
HP: 0002633
Vasculitis
0/20
HP: 0002652
Skeletal dysplasia
0/20
HP: 0002665
Lymphoma
0/20
HP: 0002719
Recurrent infections
0/20
HP: 0002720
Decreased circulating IgA level
0/20
HP: 0002795
Functional respiratory abnormality
0/20
HP: 0002829
Arthralgia
0/20
HP: 0002846
Abnormal B cell morphology
0/20
HP: 0002901
Hypocalcemia
0/20
HP: 0002904
Hyperbilirubinemia
0/20
HP: 0002921
Abnormality of the cerebrospinal fluid
0/20
HP: 0002948
Vertebral fusion
0/20
HP: 0003006
Neuroblastoma
0/20
HP: 0003111
Abnormal blood ion concentration
0/20
HP: 0003117
Abnormal circulating hormone level
0/20
HP: 0003125
Reduced factor VIII activity
0/20
HP: 0003130
Abnormal peripheral myelination
0/20
HP: 0003139
Panhypogammaglobulinemia
0/20
HP: 0003212
Increased circulating total IgE level
0/20
HP: 0003256
Abnormality of the coagulation cascade
0/20
HP: 0003265
Neonatal hyperbilirubinemia
0/20
HP: 0003271
Visceromegaly
0/20
HP: 0003287
Abnormality of mitochondrial metabolism
0/20
HP: 0003454
Platelet antibody positive
0/20
HP: 0003468
Abnormal vertebral morphology
0/20
HP: 0003641
Hemoglobinuria
0/20
HP: 0003645
Prolonged partial thromboplastin time
0/20
HP: 0004313
Decreased antibody level in blood
0/20
HP: 0004315
Decreased circulating IgG level
0/20
HP: 0004322
Short stature
0/20
HP: 0004323
Abnormality of body weight
0/20
HP: 0004325
Decreased body weight
0/20
HP: 0004363
Abnormal circulating calcium concentration
0/20
HP: 0004376
Neuroblastic tumor
0/20
HP: 0004378
Abnormality of the anus
0/20
HP: 0004395
Malnutrition
0/20
HP: 0004396
Poor appetite
0/20
HP: 0004398
Peptic ulcer
0/20
HP: 0004429
Recurrent viral infections
0/20
HP: 0004430
Severe combined immunodeficiency
0/20
HP: 0004432
Agammaglobulinemia
0/20
HP: 0004434
C8 deficiency
0/20
HP: 0004446
Stomatocytosis
0/20
HP: 0004796
Gastrointestinal obstruction
0/20
HP: 0004820
Acute myelomonocytic leukemia
0/20
HP: 0004823
Anisopoikilocytosis
0/20
HP: 0004828
Refractory anemia with ringed sideroblasts
0/20
HP: 0004841
Reduced factor XII activity
0/20
HP: 0004844
Coombs-positive hemolytic anemia
0/20
HP: 0004846
Prolonged bleeding after surgery
0/20
HP: 0004854
Intermittent thrombocytopenia
0/20
HP: 0004861
Refractory macrocytic anemia
0/20
HP: 0004914
Recurrent infantile hypoglycemia
0/20
HP: 0004941
Extrahepatic portal hypertension
0/20
HP: 0005059
Arthralgia/arthritis
0/20
HP: 0005214
Intestinal obstruction
0/20
HP: 0005288
Abnormality of the nares
0/20
HP: 0005306
Capillary hemangioma
0/20
HP: 0005353
Recurrent herpes
0/20
HP: 0005359
Aplasia of the thymus
0/20
HP: 0005363
Humoral immunodeficiency
0/20
HP: 0005365
Severe B lymphocytopenia
0/20
HP: 0005368
Abnormality of humoral immunity
0/20
HP: 0005372
Abnormality of B cell physiology
0/20
HP: 0005374
Cellular immunodeficiency
0/20
HP: 0005387
Combined immunodeficiency
0/20
HP: 0005406
Recurrent bacterial skin infections
0/20
HP: 0005415
Decreased proportion of CD8-positive T cells
0/20
HP: 0005420
Recurrent gram-negative bacterial infections
0/20
HP: 0005422
Absence of CD8-positive T cells
0/20
HP: 0005425
Recurrent sinopulmonary infections
0/20
HP: 0005453
Absent/hypoplastic paranasal sinuses
0/20
HP: 0005506
Chronic myelogenous leukemia
0/20
HP: 0005520
Chronic disseminated intravascular coagulation
0/20
HP: 0005521
Disseminated intravascular coagulation
0/20
HP: 0005522
Pyridoxine-responsive sideroblastic anemia
0/20
HP: 0005527
Reduced kininogen activity
0/20
HP: 0005537
Decreased mean platelet volume
0/20
HP: 0005541
Congenital agranulocytosis
0/20
HP: 0005559
Abnormality of the kinin-kallikrein system
0/20
HP: 0005599
Hypopigmentation of hair
0/20
HP: 0005650
Cutaneous syndactyly between fingers 2 and 5
0/20
HP: 0005775
Multiple skeletal anomalies
0/20
HP: 0005828
Transient pulmonary infiltrates
0/20
HP: 0006109
Absent phalangeal crease
0/20
HP: 0006143
Abnormal finger flexion creases
0/20
HP: 0006237
Prominent interphalangeal joints
0/20
HP: 0006270
Hypoplastic spleen
0/20
HP: 0006285
Hypomineralization of enamel
0/20
HP: 0006298
Prolonged bleeding after dental extraction
0/20
HP: 0006481
Abnormality of primary teeth
0/20
HP: 0006483
Abnormal number of teeth
0/20
HP: 0006530
Interstitial pulmonary abnormality
0/20
HP: 0006707
Abnormality of the hepatic vasculature
0/20
HP: 0006784
Paranasal sinus hypoplasia
0/20
HP: 0006946
Recurrent meningitis
0/20
HP: 0007165
Periventricular heterotopia
0/20
HP: 0007229
Intracerebral periventricular calcifications
0/20
HP: 0007392
Excessive wrinkled skin
0/20
HP: 0007440
Generalized hyperpigmentation
0/20
HP: 0007461
Hemangiomatosis
0/20
HP: 0007495
Prematurely aged appearance
0/20
HP: 0007499
Recurrent staphylococcal infections
0/20
HP: 0007517
Palmoplantar cutis laxa
0/20
HP: 0007605
Excessive wrinkling of palmar skin
0/20
HP: 0008151
Prolonged prothrombin time
0/20
HP: 0008318
Elevated leukocyte alkaline phosphatase
0/20
HP: 0008322
Abnormal mitochondrial morphology
0/20
HP: 0008330
Reduced von Willebrand factor activity
0/20
HP: 0008352
Impaired platelet adhesion
0/20
HP: 0008872
Feeding difficulties in infancy
0/20
HP: 0009116
Aplasia/Hypoplasia involving bones of the skull
0/20
HP: 0009120
Aplasia/Hypoplasia involving the sinuses
0/20
HP: 0009121
Abnormal axial skeleton morphology
0/20
HP: 0009122
Aplasia/hypoplasia affecting bones of the axial skeleton
0/20
HP: 0009732
Plexiform neurofibroma
0/20
HP: 0009733
Glioma
0/20
HP: 0009799
Supernumerary spleens
0/20
HP: 0009804
Reduced number of teeth
0/20
HP: 0009934
Supernumerary naris
0/20
HP: 0010052
Abnormal morphology of the proximal phalanx of the hallux
0/20
HP: 0010057
Abnormality of the phalanges of the hallux
0/20
HP: 0010059
Broad hallux phalanx
0/20
HP: 0010086
Broad proximal phalanx of the hallux
0/20
HP: 0010161
Abnormality of the phalanges of the toes
0/20
HP: 0010173
Aplasia/Hypoplasia of the phalanges of the toes
0/20
HP: 0010174
Broad phalanx of the toes
0/20
HP: 0010183
Abnormality of the middle phalanges of the toes
0/20
HP: 0010184
Abnormality of toe proximal phalanx
0/20
HP: 0010204
Broad proximal phalanx of toe
0/20
HP: 0010452
Ectopia of the spleen
0/20
HP: 0010515
Aplasia/Hypoplasia of the thymus
0/20
HP: 0010554
Cutaneous finger syndactyly
0/20
HP: 0010638
Elevated alkaline phosphatase of hepatic origin
0/20
HP: 0010647
Abnormal elasticity of skin
0/20
HP: 0010679
Elevated tissue non-specific alkaline phosphatase
0/20
HP: 0010701
Abnormal immunoglobulin level
0/20
HP: 0010704
1-2 finger syndactyly
0/20
HP: 0010745
Aplasia of the phalanges of the toes
0/20
HP: 0010876
Abnormal circulating protein level
0/20
HP: 0010927
Abnormal blood inorganic cation concentration
0/20
HP: 0010929
Abnormal blood cation concentration
0/20
HP: 0010974
Abnormal myeloid leukocyte morphology
0/20
HP: 0010975
Abnormal B cell count
0/20
HP: 0010976
B lymphocytopenia
0/20
HP: 0010989
Abnormality of the intrinsic pathway
0/20
HP: 0010990
Abnormality of the common coagulation pathway
0/20
HP: 0011017
Abnormal cellular physiology
0/20
HP: 0011032
Abnormality of fluid regulation
0/20
HP: 0011034
Amyloidosis
0/20
HP: 0011063
Abnormality of incisor morphology
0/20
HP: 0011096
Peripheral demyelination
0/20
HP: 0011109
Chronic sinusitis
0/20
HP: 0011132
Chronic furunculosis
0/20
HP: 0011356
Regional abnormality of skin
0/20
HP: 0011358
Generalized hypopigmentation of hair
0/20
HP: 0011362
Abnormal hair quantity
0/20
HP: 0011384
Abnormality of the internal auditory canal
0/20
HP: 0011385
Absent internal auditory canal
0/20
HP: 0011390
Morphological abnormality of the inner ear
0/20
HP: 0011446
Abnormality of higher mental function
0/20
HP: 0011450
Unusual CNS infection
0/20
HP: 0011458
Abdominal symptom
0/20
HP: 0011821
Abnormality of facial skeleton
0/20
HP: 0011830
Abnormal oral mucosa morphology
0/20
HP: 0011837
Partial IgA deficiency
0/20
HP: 0011843
Abnormality of skeletal physiology
0/20
HP: 0011858
Reduced factor IX activity
0/20
HP: 0011869
Abnormal platelet function
0/20
HP: 0011874
Heparin-induced thrombocytopenia
0/20
HP: 0011875
Abnormal platelet morphology
0/20
HP: 0011876
Abnormal platelet volume
0/20
HP: 0011880
Acute disseminated intravascular coagulation
0/20
HP: 0011898
Abnormality of circulating fibrinogen
0/20
HP: 0011901
Dysfibrinogenemia
0/20
HP: 0011944
Small vessel vasculitis
0/20
HP: 0011947
Respiratory tract infection
0/20
HP: 0011965
Abnormal circulating citrulline concentration
0/20
HP: 0011966
Elevated plasma citrulline
0/20
HP: 0011968
Feeding difficulties
0/20
HP: 0011974
Myelofibrosis
0/20
HP: 0011991
Abnormal neutrophil count
0/20
HP: 0012103
Abnormality of the mitochondrion
0/20
HP: 0012131
Abnormal number of erythroid precursors
0/20
HP: 0012132
Erythroid hyperplasia
0/20
HP: 0012135
Abnormal granulocytopoietic cell morphology
0/20
HP: 0012146
Abnormality of von Willebrand factor
0/20
HP: 0012150
Single lineage myelodysplasia
0/20
HP: 0012156
Hemophagocytosis
0/20
HP: 0012175
Resistance to activated protein C
0/20
HP: 0012200
Abnormality of prothrombin
0/20
HP: 0012223
Splenic rupture
0/20
HP: 0012234
Agranulocytosis
0/20
HP: 0012235
Drug-induced agranulocytosis
0/20
HP: 0012239
Atransferrinemia
0/20
HP: 0012280
Hepatic amyloidosis
0/20
HP: 0012316
Fibrous tissue neoplasm
0/20
HP: 0012372
Abnormal eye morphology
0/20
HP: 0012373
Abnormal eye physiology
0/20
HP: 0012447
Abnormal myelination
0/20
HP: 0012475
Decreased circulating level of specific antibody
0/20
HP: 0012524
Abnormal platelet shape
0/20
HP: 0012539
Non-Hodgkin lymphoma
0/20
HP: 0012543
Hemosiderinuria
0/20
HP: 0012546
Skewed maternal X inactivation
0/20
HP: 0012575
Abnormal nephron morphology
0/20
HP: 0012638
Abnormal nervous system physiology
0/20
HP: 0012724
Upper eyelid edema
0/20
HP: 0012880
Abnormality of the labia minora
0/20
HP: 0020064
Abnormal eosinophil count
0/20
HP: 0020071
Viremia
0/20
HP: 0020080
Erythrocyte inclusion bodies
0/20
HP: 0020081
Pappenheimer bodies
0/20
HP: 0020100
Unusual fungal infection
0/20
HP: 0020179
Abnormal haptoglobin level
0/20
HP: 0020186
Multilobulated spleen
0/20
HP: 0025031
Abnormality of the digestive system
0/20
HP: 0025033
Abnormality of digestive system morphology
0/20
HP: 0025245
Cutaneous cyst
0/20
HP: 0025326
Retinal arterial occlusion
0/20
HP: 0025342
Central retinal artery occlusion
0/20
HP: 0025354
Abnormal cellular phenotype
0/20
HP: 0025408
Abnormal spleen morphology
0/20
HP: 0025409
Abnormal spleen physiology
0/20
HP: 0025429
Abnormal cry
0/20
HP: 0025430
High-pitched cry
0/20
HP: 0025456
Abnormal CSF protein level
0/20
HP: 0025458
Decreased CSF albumin concentration
0/20
HP: 0025465
Abnormal circulating beta globulin level
0/20
HP: 0025539
Abnormal B cell subset distribution
0/20
HP: 0025615
Abscess
0/20
HP: 0025639
Increased urinary zinc level
0/20
HP: 0025640
Abnormal urinary mineral level
0/20
HP: 0030057
Autoimmune antibody positivity
0/20
HP: 0030060
Nervous tissue neoplasm
0/20
HP: 0030061
Neuroectodermal neoplasm
0/20
HP: 0030063
Neuroepithelial neoplasm
0/20
HP: 0030065
Primitive neuroectodermal tumor
0/20
HP: 0030067
Peripheral primitive neuroectodermal neoplasm
0/20
HP: 0030069
Primary central nervous system lymphoma
0/20
HP: 0030082
Abnormal drinking behavior
0/20
HP: 0030166
Night sweats
0/20
HP: 0030318
Angular cheilitis
0/20
HP: 0030402
Abnormal platelet aggregation
0/20
HP: 0030601
Abnormal posterior segment imaging
0/20
HP: 0030603
Abnormal optical coherence tomography
0/20
HP: 0030669
Abnormal ocular adnexa morphology
0/20
HP: 0030680
Abnormality of cardiovascular system morphology
0/20
HP: 0030780
Abnormality of the protein C anticoagulant pathway
0/20
HP: 0030809
Abnormal tongue morphology
0/20
HP: 0030810
Abnormal tongue physiology
0/20
HP: 0030811
Tongue pain
0/20
HP: 0030829
Abnormal breath sound
0/20
HP: 0030895
Abnormal gastrointestinal motility
0/20
HP: 0030914
Abnormal peristalsis
0/20
HP: 0031071
Abnormal endocrine morphology
0/20
HP: 0031160
Myelokathexis
0/20
HP: 0031244
Swollen lip
0/20
HP: 0031364
Ecchymosis
0/20
HP: 0031365
Macular purpura
0/20
HP: 0031404
Impaired antigen-specific response
0/20
HP: 0031409
Abnormal lymphocyte physiology
0/20
HP: 0031466
Impairment in personality functioning
0/20
HP: 0031635
Anomalous origin of the left common carotid artery from the brachiocephalic artery
0/20
HP: 0031696
Disseminated viral infection
0/20
HP: 0031816
Abnormal oral morphology
0/20
HP: 0031863
Bloodstream infectious agent
0/20
HP: 0031910
Abnormal cranial nerve physiology
0/20
HP: 0032039
Abnormality of the ocular adnexa
0/20
HP: 0032101
Unusual infection
0/20
HP: 0032158
Unusual infection by anatomical site
0/20
HP: 0032162
Unusual skin infection
0/20
HP: 0032163
Molluscum contagiosum
0/20
HP: 0032169
Severe infection
0/20
HP: 0032179
Abnormal circulating globulin level
0/20
HP: 0032185
Disseminated molluscum contagiosum
0/20
HP: 0032198
Decreased prothrombin time
0/20
HP: 0032199
Abnormal prothrombin time
0/20
HP: 0032248
Persistent viremia
0/20
HP: 0032253
Eosinophilic granuloma
0/20
HP: 0032255
Opportunistic fungal infection
0/20
HP: 0032309
Abnormal granulocyte count
0/20
HP: 0032366
Positive direct antiglobulin test
0/20
HP: 0032385
Abnormal circulating transferrin level
0/20
HP: 0032388
Periventricular nodular heterotopia
0/20
HP: 0032550
Howell-Jolly bodies
0/20
HP: 0040075
Hypopituitarism
0/20
HP: 0040088
Abnormal lymphocyte count
0/20
HP: 0040133
Abnormal serum ferritin
0/20
HP: 0040142
Reduced 5-oxoprolinase activity
0/20
HP: 0040202
Abnormal consumption behavior
0/20
HP: 0040211
Abnormality of the skin of the palm
0/20
HP: 0040223
Pulmonary hemorrhage
0/20
HP: 0040224
Abnormality of fibrinolysis
0/20
HP: 0040236
Hyperfibrinolysis
0/20
HP: 0040241
Increased RIPA
0/20
HP: 0045010
Abnormality of peripheral nerves
0/20
HP: 0045026
Abnormality of the mediastinum
0/20
HP: 0045027
Abnormality of the thoracic cavity
0/20
HP: 0045029
Eosinophilic fasciitis
0/20
HP: 0045044
Decreased serum complement C4b
0/20
HP: 0045073
Serositis
0/20
HP: 0100007
Neoplasm of the peripheral nervous system
0/20
HP: 0100521
Neoplasm of the thymus
0/20
HP: 0100522
Thymoma
0/20
HP: 0100533
Inflammatory abnormality of the eye
0/20
HP: 0100540
Palpebral edema
0/20
HP: 0100547
Abnormality of forebrain morphology
0/20
HP: 0100594
Esophageal web
0/20
HP: 0100639
Erectile dysfunction
0/20
HP: 0100678
Premature skin wrinkling
0/20
HP: 0100724
Hypercoagulability
0/20
HP: 0100727
Histiocytosis
0/20
HP: 0100770
Hyperperistalsis
0/20
HP: 0100809
Scalp tenderness
0/20
HP: 0100827
Lymphocytosis
0/20
HP: 0100836
Malignant neoplasm of the central nervous system
0/20
HP: 0100871
Abnormality of the palm
0/20
HP: 0100892
Abnormality of the xiphoid process
0/20
HP: 0100893
Prominent xiphoid process
0/20
HP: 0200029
Vasculitis in the skin
0/20
HP: 0200034
Papule
0/20
HP: 0200040
Epidermoid cyst
0/20
HP: 0410006
Abnormality of ophthalmic artery
0/20
HP: 0410008
Abnormality of the peripheral nervous system
0/20
HP: 0410042
Abnormal liver morphology
0/20
HP: 0410049
Abnormality of radial ray
0/20
HP: 0410240
Abnormal IgA level
0/20
HP: 0410241
Abnormal IgE level
0/20
HP: 0410268
Spleen hemangioma
0/20
HP: 0430021
Abnormal common carotid artery morphology
0/20
HP: 0500165
Abnormal blood oxygen level
0/20
HP: 0500238
Abnormal CSF albumin concentration
0/20
HP: 3000032
Abnormality of central retinal artery
0/20
HP: 3000036
Abnormality of head blood vessel
0/20
HP: 3000050
Abnormality of odontoid tissue
0/20
HP: 3000062
Abnormal internal carotid artery morphology
0/20