Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Chapter3

Case/Control GWAS

GWAS of Chapter3

Statistics

Case Control
34091 426115

Top SNP Information

Associated 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