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Top SNP Information Show Table

Associated Phenotypes ^ⓘ Shared SNP phenotypes No shared SNP phenotypes

ID	Name	Top Correlation
HP: 0000078	Abnormality of the genital system	1/20
HP: 0000118	Phenotypic abnormality	2/20
HP: 0000119	Abnormality of the genitourinary system	2/20
HP: 0000152	Abnormality of head or neck	2/20
HP: 0000234	Abnormality of the head	2/20
HP: 0000282	Facial edema	4/20
HP: 0000356	Abnormality of the outer ear	7/20
HP: 0000359	Abnormality of the inner ear	3/20
HP: 0000364	Hearing abnormality	12/20
HP: 0000365	Hearing impairment	12/20
HP: 0000370	Abnormality of the middle ear	4/20
HP: 0000377	Abnormality of the pinna	6/20
HP: 0000383	Abnormality of periauricular region	1/20
HP: 0000405	Conductive hearing impairment	11/20
HP: 0000407	Sensorineural hearing impairment	15/20
HP: 0000492	Abnormal eyelid morphology	1/20
HP: 0000496	Abnormality of eye movement	1/20
HP: 0000502	Abnormal conjunctiva morphology	3/20
HP: 0000504	Abnormality of vision	1/20
HP: 0000505	Visual impairment	3/20
HP: 0000589	Coloboma	4/20
HP: 0000598	Abnormality of the ear	9/20
HP: 0000606	Abnormality of the periorbital region	3/20
HP: 0000629	Periorbital fullness	4/20
HP: 0000640	Gaze-evoked nystagmus	2/20
HP: 0000707	Abnormality of the nervous system	1/20
HP: 0000924	Abnormality of the skeletal system	2/20
HP: 0000929	Abnormal skull morphology	1/20
HP: 0000940	Abnormal diaphysis morphology	2/20
HP: 0000964	Eczema	6/20
HP: 0001055	Erysipelas	5/20
HP: 0001072	Thickened skin	1/20
HP: 0001155	Abnormality of the hand	5/20
HP: 0001159	Syndactyly	8/20
HP: 0001167	Abnormality of finger	4/20
HP: 0001287	Meningitis	2/20
HP: 0001298	Encephalopathy	3/20
HP: 0001311	Abnormal nervous system electrophysiology	1/20
HP: 0001332	Dystonia	2/20
HP: 0001367	Abnormal joint morphology	2/20
HP: 0001369	Arthritis	2/20
HP: 0001405	Periportal fibrosis	1/20
HP: 0001595	Abnormal hair morphology	5/20
HP: 0001608	Abnormality of the voice	1/20
HP: 0001626	Abnormality of the cardiovascular system	1/20
HP: 0001627	Abnormal heart morphology	1/20
HP: 0001679	Abnormal aortic morphology	5/20
HP: 0001739	Abnormality of the nasopharynx	5/20
HP: 0001760	Abnormality of the foot	2/20
HP: 0001780	Abnormality of toe	4/20
HP: 0001844	Abnormality of the hallux	5/20
HP: 0001888	Lymphopenia	1/20
HP: 0001892	Abnormal bleeding	2/20
HP: 0001939	Abnormality of metabolism/homeostasis	2/20
HP: 0001999	Abnormal facial shape	3/20
HP: 0002011	Morphological central nervous system abnormality	2/20
HP: 0002063	Rigidity	8/20
HP: 0002076	Migraine	2/20
HP: 0002086	Abnormality of the respiratory system	2/20
HP: 0002088	Abnormal lung morphology	2/20
HP: 0002183	Phonophobia	3/20
HP: 0002205	Recurrent respiratory infections	3/20
HP: 0002242	Abnormal intestine morphology	2/20
HP: 0002244	Abnormality of the small intestine	3/20
HP: 0002500	Abnormality of the cerebral white matter	2/20
HP: 0002574	Episodic abdominal pain	6/20
HP: 0002597	Abnormality of the vasculature	1/20
HP: 0002644	Abnormality of pelvic girdle bone morphology	2/20
HP: 0002664	Neoplasm	1/20
HP: 0002683	Abnormality of the calvaria	1/20
HP: 0002693	Abnormality of the skull base	2/20
HP: 0002715	Abnormality of the immune system	1/20
HP: 0002716	Lymphadenopathy	3/20
HP: 0002718	Recurrent bacterial infections	1/20
HP: 0002730	Chronic noninfectious lymphadenopathy	1/20
HP: 0002733	Abnormality of the lymph nodes	2/20
HP: 0002754	Osteomyelitis	7/20
HP: 0002788	Recurrent upper respiratory tract infections	4/20
HP: 0002793	Abnormal pattern of respiration	4/20
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	2/20
HP: 0002843	Abnormal T cell morphology	4/20
HP: 0002955	Granulomatosis	3/20
HP: 0003011	Abnormality of the musculature	1/20
HP: 0003330	Abnormal bone structure	2/20
HP: 0003549	Abnormality of connective tissue	5/20
HP: 0004311	Abnormal macrophage morphology	2/20
HP: 0004332	Abnormal lymphocyte morphology	2/20
HP: 0004372	Reduced consciousness/confusion	1/20
HP: 0004377	Hematological neoplasm	3/20
HP: 0004406	Spontaneous, recurrent epistaxis	1/20
HP: 0004464	Postauricular pit	1/20
HP: 0005339	Abnormality of complement system	3/20
HP: 0005403	Decrease in T cell count	2/20
HP: 0005922	Abnormal hand morphology	5/20
HP: 0006101	Finger syndactyly	8/20
HP: 0006504	obsolete Anomaly of the limb diaphyses morphology	2/20
HP: 0006824	Cranial nerve paralysis	1/20
HP: 0007302	Bipolar affective disorder	2/20
HP: 0008609	Morphological abnormality of the middle ear	2/20
HP: 0009115	Aplasia/hypoplasia involving the skeleton	2/20
HP: 0009797	Cholesteatoma	5/20
HP: 0010051	Deviation of the hallux	1/20
HP: 0010606	Hordeolum	4/20
HP: 0010607	Hordeolum externum	5/20
HP: 0010622	Neoplasm of the skeletal system	7/20
HP: 0010628	Facial palsy	1/20
HP: 0010720	Abnormal hair pattern	8/20
HP: 0010732	Nodular changes affecting the eyelids	5/20
HP: 0010827	Abnormality of the seventh cranial nerve	1/20
HP: 0010978	Abnormality of immune system physiology	2/20
HP: 0010993	Abnormality of the cerebral subcortex	2/20
HP: 0011004	Abnormal systemic arterial morphology	6/20
HP: 0011006	Abnormal morphology of the musculature of the neck	2/20
HP: 0011024	Abnormality of the gastrointestinal tract	7/20
HP: 0011028	Abnormality of blood circulation	2/20
HP: 0011029	Internal hemorrhage	2/20
HP: 0011110	Tonsillitis	1/20
HP: 0011121	Abnormality of skin morphology	2/20
HP: 0011122	Abnormality of skin physiology	4/20
HP: 0011123	Inflammatory abnormality of the skin	4/20
HP: 0011138	Abnormality of skin adnexa morphology	5/20
HP: 0011297	Abnormal digit morphology	3/20
HP: 0011314	Abnormality of long bone morphology	1/20
HP: 0011338	Abnormality of mouth shape	5/20
HP: 0011355	Localized skin lesion	4/20
HP: 0011360	Acquired abnormal hair pattern	5/20
HP: 0011368	Epidermal thickening	1/20
HP: 0011389	Functional abnormality of the inner ear	3/20
HP: 0011442	Abnormal central motor function	1/20
HP: 0011444	Decorticate rigidity	8/20
HP: 0011452	Functional abnormality of the middle ear	11/20
HP: 0011793	Neoplasm by anatomical site	1/20
HP: 0011799	Abnormality of facial soft tissue	3/20
HP: 0011804	Abnormal muscle physiology	1/20
HP: 0011805	Abnormal skeletal muscle morphology	2/20
HP: 0011839	Abnormal T cell count	4/20
HP: 0011842	Abnormality of skeletal morphology	2/20
HP: 0011844	Abnormal appendicular skeleton morphology	2/20
HP: 0011849	Abnormal bone ossification	1/20
HP: 0011899	Hyperfibrinogenemia	2/20
HP: 0012252	Abnormal respiratory system morphology	2/20
HP: 0012303	Abnormal aortic arch morphology	1/20
HP: 0012337	Abnormal homeostasis	1/20
HP: 0012387	Bronchitis	2/20
HP: 0012388	Acute bronchitis	1/20
HP: 0012395	Seasonal allergy	3/20
HP: 0012443	Abnormality of brain morphology	2/20
HP: 0012531	Pain	1/20
HP: 0012639	Abnormal nervous system morphology	1/20
HP: 0012647	Abnormal inflammatory response	5/20
HP: 0012649	Increased inflammatory response	5/20
HP: 0012718	Morphological abnormality of the gastrointestinal tract	5/20
HP: 0012725	Cutaneous syndactyly	8/20
HP: 0012759	Neurodevelopmental abnormality	2/20
HP: 0012780	Neoplasm of the ear	4/20
HP: 0025015	Abnormal vascular morphology	6/20
HP: 0025032	Abnormality of digestive system physiology	1/20
HP: 0025084	Folliculitis	1/20
HP: 0025112	Sound sensitivity	3/20
HP: 0025142	Constitutional symptom	2/20
HP: 0025439	Pharyngitis	1/20
HP: 0030014	Female sexual dysfunction	3/20
HP: 0030017	Vaginismus	1/20
HP: 0030178	Abnormality of central nervous system electrophysiology	3/20
HP: 0030313	Abnormal periosteum morphology	1/20
HP: 0030319	Weakness of facial musculature	9/20
HP: 0030766	Ear pain	2/20
HP: 0030831	Rhonchi	3/20
HP: 0030962	Abnormal morphology of the great vessels	1/20
HP: 0031283	Tufted hairs	3/20
HP: 0031292	Cutaneous abscess	3/20
HP: 0031458	Adenoiditis	5/20
HP: 0031703	Abnormal ear morphology	10/20
HP: 0031704	Abnormal ear physiology	6/20
HP: 0032148	Episodic pain	6/20
HP: 0040064	Abnormality of limbs	2/20
HP: 0040068	Abnormality of limb bone	2/20
HP: 0040069	Abnormal lower limb bone morphology	2/20
HP: 0040165	Periostitis	1/20
HP: 0040166	Abnormality of the periosteum	1/20
HP: 0100022	Abnormality of movement	2/20
HP: 0100277	Periauricular skin pits	1/20
HP: 0100498	Deviation of toes	2/20
HP: 0100536	Abnormality of the fascia	3/20
HP: 0100537	Fasciitis	3/20
HP: 0100539	Periorbital edema	5/20
HP: 0100568	Neoplasm of the endocrine system	6/20
HP: 0100634	Neuroendocrine neoplasm	7/20
HP: 0100658	Cellulitis	6/20
HP: 0100754	Mania	2/20
HP: 0100777	Exostoses	7/20
HP: 0100799	Neoplasm of the middle ear	5/20
HP: 0200036	Skin nodule	3/20
HP: 3000033	Abnormality of nasopharyngeal adenoids	5/20

ID	Name	Top Correlation
HP: 0000080	Abnormality of reproductive system physiology	0/20
HP: 0000153	Abnormality of the mouth	0/20
HP: 0000163	Abnormal oral cavity morphology	0/20
HP: 0000172	Abnormality of the uvula	0/20
HP: 0000174	Abnormal palate morphology	0/20
HP: 0000193	Bifid uvula	0/20
HP: 0000245	Abnormality of the paranasal sinuses	0/20
HP: 0000246	Sinusitis	0/20
HP: 0000255	Acute sinusitis	0/20
HP: 0000264	Abnormality of the mastoid	0/20
HP: 0000265	Mastoiditis	0/20
HP: 0000271	Abnormality of the face	0/20
HP: 0000301	Abnormality of facial musculature	0/20
HP: 0000309	Abnormality of the midface	0/20
HP: 0000315	Abnormality of the orbital region	0/20
HP: 0000360	Tinnitus	0/20
HP: 0000362	Otosclerosis	0/20
HP: 0000366	Abnormality of the nose	0/20
HP: 0000371	Acute otitis media	0/20
HP: 0000372	Abnormality of the auditory canal	0/20
HP: 0000375	Abnormal cochlea morphology	0/20
HP: 0000388	Otitis media	0/20
HP: 0000389	Chronic otitis media	0/20
HP: 0000402	Stenosis of the external auditory canal	0/20
HP: 0000403	Recurrent otitis media	0/20
HP: 0000408	Progressive sensorineural hearing impairment	0/20
HP: 0000410	Mixed hearing impairment	0/20
HP: 0000415	Abnormality of the choanae	0/20
HP: 0000421	Epistaxis	0/20
HP: 0000453	Choanal atresia	0/20
HP: 0000464	Abnormality of the neck	0/20
HP: 0000473	Torticollis	0/20
HP: 0000478	Abnormality of the eye	0/20
HP: 0000572	Visual loss	0/20
HP: 0000600	Abnormality of the pharynx	0/20
HP: 0000614	Abnormal nasolacrimal system morphology	0/20
HP: 0000639	Nystagmus	0/20
HP: 0000666	Horizontal nystagmus	0/20
HP: 0000708	Behavioral abnormality	0/20
HP: 0000733	Stereotypy	0/20
HP: 0000750	Delayed speech and language development	0/20
HP: 0000759	Abnormal peripheral nervous system morphology	0/20
HP: 0000851	Congenital hypothyroidism	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: 0001036	Parakeratosis	0/20
HP: 0001251	Ataxia	0/20
HP: 0001291	Abnormal cranial nerve morphology	0/20
HP: 0001293	Cranial nerve compression	0/20
HP: 0001310	Dysmetria	0/20
HP: 0001324	Muscle weakness	0/20
HP: 0001328	Specific learning disability	0/20
HP: 0001336	Myoclonus	0/20
HP: 0001392	Abnormality of the liver	0/20
HP: 0001395	Hepatic fibrosis	0/20
HP: 0001574	Abnormality of the integument	0/20
HP: 0001581	Recurrent skin infections	0/20
HP: 0001609	Hoarse voice	0/20
HP: 0001637	Abnormal myocardium morphology	0/20
HP: 0001730	Progressive hearing impairment	0/20
HP: 0001751	Vestibular dysfunction	0/20
HP: 0001756	Vestibular hypofunction	0/20
HP: 0001863	Toe clinodactyly	0/20
HP: 0001871	Abnormality of blood and blood-forming tissues	0/20
HP: 0001879	Abnormal eosinophil morphology	0/20
HP: 0001880	Eosinophilia	0/20
HP: 0001881	Abnormal leukocyte morphology	0/20
HP: 0001882	Leukopenia	0/20
HP: 0001909	Leukemia	0/20
HP: 0001911	Abnormal granulocyte morphology	0/20
HP: 0001928	Abnormality of coagulation	0/20
HP: 0001974	Leukocytosis	0/20
HP: 0002012	Abnormality of the abdominal organs	0/20
HP: 0002027	Abdominal pain	0/20
HP: 0002060	Abnormal cerebral morphology	0/20
HP: 0002167	Neurological speech impairment	0/20
HP: 0002180	Neurodegeneration	0/20
HP: 0002315	Headache	0/20
HP: 0002321	Vertigo	0/20
HP: 0002352	Leukoencephalopathy	0/20
HP: 0002442	Dyscalculia	0/20
HP: 0002474	Expressive language delay	0/20
HP: 0002516	Increased intracranial pressure	0/20
HP: 0002633	Vasculitis	0/20
HP: 0002648	Abnormality of calvarial morphology	0/20
HP: 0002665	Lymphoma	0/20
HP: 0002668	Paraganglioma	0/20
HP: 0002719	Recurrent infections	0/20
HP: 0002728	Chronic mucocutaneous candidiasis	0/20
HP: 0002737	Thick skull base	0/20
HP: 0002740	Recurrent E. coli infections	0/20
HP: 0002763	Abnormal cartilage morphology	0/20
HP: 0002791	Hypoventilation	0/20
HP: 0002795	Functional respiratory abnormality	0/20
HP: 0002840	Lymphadenitis	0/20
HP: 0002841	Recurrent fungal infections	0/20
HP: 0002864	Paraganglioma of head and neck	0/20
HP: 0002921	Abnormality of the cerebrospinal fluid	0/20
HP: 0002926	Abnormality of thyroid physiology	0/20
HP: 0003001	Glomus jugular tumor	0/20
HP: 0003256	Abnormality of the coagulation cascade	0/20
HP: 0003468	Abnormal vertebral morphology	0/20
HP: 0003470	Paralysis	0/20
HP: 0004305	Involuntary movements	0/20
HP: 0004348	Abnormality of bone mineral density	0/20
HP: 0004373	Focal dystonia	0/20
HP: 0004375	Neoplasm of the nervous system	0/20
HP: 0004426	Abnormality of the cheek	0/20
HP: 0004452	Abnormality of the middle ear ossicles	0/20
HP: 0004459	Exostosis of the external auditory canal	0/20
HP: 0004880	Respiratory infections in early life	0/20
HP: 0005019	Diaphyseal thickening	0/20
HP: 0005216	Impaired mastication	0/20
HP: 0005368	Abnormality of humoral immunity	0/20
HP: 0005420	Recurrent gram-negative bacterial infections	0/20
HP: 0005453	Absent/hypoplastic paranasal sinuses	0/20
HP: 0005464	Craniofacial osteosclerosis	0/20
HP: 0005482	Abnormality of the alternative complement pathway	0/20
HP: 0005534	Transient myeloproliferative syndrome	0/20
HP: 0005547	Myeloproliferative disorder	0/20
HP: 0005650	Cutaneous syndactyly between fingers 2 and 5	0/20
HP: 0005746	Osteosclerosis of the base of the skull	0/20
HP: 0006846	Acute encephalopathy	0/20
HP: 0006897	Cranial nerve VI palsy	0/20
HP: 0006934	Congenital nystagmus	0/20
HP: 0006943	Diffuse spongiform leukoencephalopathy	0/20
HP: 0006946	Recurrent meningitis	0/20
HP: 0006958	Abnormal auditory evoked potentials	0/20
HP: 0006965	Acute necrotizing encephalopathy	0/20
HP: 0007209	Facial paralysis	0/20
HP: 0007274	Recurrent bacterial meningitis	0/20
HP: 0007286	Horizontal jerk nystagmus	0/20
HP: 0007367	Atrophy/Degeneration affecting the central nervous system	0/20
HP: 0007670	Abnormal vestibulo-ocular reflex	0/20
HP: 0007892	Hypoplasia of the lacrimal punctum	0/20
HP: 0008066	Abnormal blistering of the skin	0/20
HP: 0008069	Neoplasm of the skin	0/20
HP: 0008223	Compensated hypothyroidism	0/20
HP: 0008513	Bilateral conductive hearing impairment	0/20
HP: 0008519	Abnormality of the coccyx	0/20
HP: 0008527	Congenital sensorineural hearing impairment	0/20
HP: 0008542	Low-frequency hearing loss	0/20
HP: 0008554	Cochlear malformation	0/20
HP: 0008573	Low-frequency sensorineural hearing impairment	0/20
HP: 0008591	Congenital conductive hearing impairment	0/20
HP: 0008598	Mild conductive hearing impairment	0/20
HP: 0008619	Bilateral sensorineural hearing impairment	0/20
HP: 0008625	Severe sensorineural hearing impairment	0/20
HP: 0008628	Abnormality of the stapes	0/20
HP: 0008629	Pulsatile tinnitus	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: 0009591	Abnormality of the vestibulocochlear nerve	0/20
HP: 0009704	Chronic CSF lymphocytosis	0/20
HP: 0009911	Abnormal temporal bone morphology	0/20
HP: 0010307	Stridor	0/20
HP: 0010530	Palatal myoclonus	0/20
HP: 0010532	Paroxysmal vertigo	0/20
HP: 0010542	Vestibular nystagmus	0/20
HP: 0010544	Vertical nystagmus	0/20
HP: 0010554	Cutaneous finger syndactyly	0/20
HP: 0010775	Vascular ring	0/20
HP: 0010974	Abnormal myeloid leukocyte morphology	0/20
HP: 0010987	Abnormal cellular immune system morphology	0/20
HP: 0010990	Abnormality of the common coagulation pathway	0/20
HP: 0011001	Increased bone mineral density	0/20
HP: 0011025	Abnormal cardiovascular system physiology	0/20
HP: 0011032	Abnormality of fluid regulation	0/20
HP: 0011108	Recurrent sinusitis	0/20
HP: 0011109	Chronic sinusitis	0/20
HP: 0011348	Abnormality of the sixth cranial nerve	0/20
HP: 0011349	Abducens palsy	0/20
HP: 0011370	Recurrent cutaneous fungal infections	0/20
HP: 0011373	Incomplete partition of the cochlea	0/20
HP: 0011376	Morphological abnormality of the vestibule of the inner ear	0/20
HP: 0011380	Morphological abnormality of the semicircular canal	0/20
HP: 0011381	Aplasia of the semicircular canal	0/20
HP: 0011384	Abnormality of the internal auditory canal	0/20
HP: 0011386	Narrow internal auditory canal	0/20
HP: 0011390	Morphological abnormality of the inner ear	0/20
HP: 0011443	Abnormality of coordination	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: 0011472	Abnormality of small intestinal villus morphology	0/20
HP: 0011473	Villous atrophy	0/20
HP: 0011477	Upbeat nystagmus	0/20
HP: 0011479	Abnormal lacrimal punctum morphology	0/20
HP: 0011587	Abnormal branching pattern of the aortic arch	0/20
HP: 0011821	Abnormality of facial skeleton	0/20
HP: 0011843	Abnormality of skeletal physiology	0/20
HP: 0011893	Abnormal leukocyte count	0/20
HP: 0011898	Abnormality of circulating fibrinogen	0/20
HP: 0011947	Respiratory tract infection	0/20
HP: 0012179	Craniofacial dystonia	0/20
HP: 0012190	T-cell lymphoma	0/20
HP: 0012192	Cutaneous T-cell lymphoma	0/20
HP: 0012203	Onychomycosis	0/20
HP: 0012204	Recurrent vulvovaginal candidiasis	0/20
HP: 0012229	CSF pleocytosis	0/20
HP: 0012322	Perifolliculitis	0/20
HP: 0012372	Abnormal eye morphology	0/20
HP: 0012373	Abnormal eye physiology	0/20
HP: 0012393	Allergy	0/20
HP: 0012539	Non-Hodgkin lymphoma	0/20
HP: 0012547	Abnormal involuntary eye movements	0/20
HP: 0012638	Abnormal nervous system physiology	0/20
HP: 0012640	Abnormality of intracranial pressure	0/20
HP: 0012641	Decreased intracranial pressure	0/20
HP: 0012712	Mild hearing impairment	0/20
HP: 0012714	Severe hearing impairment	0/20
HP: 0012717	Severe conductive hearing impairment	0/20
HP: 0012758	Neurodevelopmental delay	0/20
HP: 0012779	Transient hearing impairment	0/20
HP: 0012799	Unilateral facial palsy	0/20
HP: 0012852	Hepatic bridging fibrosis	0/20
HP: 0020064	Abnormal eosinophil count	0/20
HP: 0020100	Unusual fungal infection	0/20
HP: 0020101	Invasive fungal infection	0/20
HP: 0020103	Invasive pulmonary aspergillosis	0/20
HP: 0020108	Unusual parasitic infection	0/20
HP: 0020123	Tympanosclerosis	0/20
HP: 0020169	Abnormal drug response	0/20
HP: 0020173	Reduced drug efficacy	0/20
HP: 0025031	Abnormality of the digestive system	0/20
HP: 0025033	Abnormality of digestive system morphology	0/20
HP: 0025268	Stuttering	0/20
HP: 0030012	Abnormal female reproductive system physiology	0/20
HP: 0030084	Clinodactyly	0/20
HP: 0030177	Abnormality of peripheral nervous system electrophysiology	0/20
HP: 0030350	Erythematous papule	0/20
HP: 0030669	Abnormal ocular adnexa morphology	0/20
HP: 0030680	Abnormality of cardiovascular system morphology	0/20
HP: 0030775	Modic type vertebral endplate changes	0/20
HP: 0030776	Modic type I vertebral endplate changes	0/20
HP: 0030787	Cerumen abnormality	0/20
HP: 0030788	Impacted cerumen	0/20
HP: 0030789	Excessive cerumen	0/20
HP: 0030829	Abnormal breath sound	0/20
HP: 0030885	Recurrent parasitic infections	0/20
HP: 0030947	Conjunctival follicles	0/20
HP: 0031002	Neuritis	0/20
HP: 0031071	Abnormal endocrine morphology	0/20
HP: 0031072	Abnormal endocrine physiology	0/20
HP: 0031321	Myocardial immune cell infiltration	0/20
HP: 0031322	Myocardial lymphocytic infiltration	0/20
HP: 0031353	Otitis media with effusion	0/20
HP: 0031466	Impairment in personality functioning	0/20
HP: 0031549	Lymphocytoma cutis	0/20
HP: 0031690	Opportunistic infection	0/20
HP: 0031691	Severe viral infection	0/20
HP: 0031696	Disseminated viral infection	0/20
HP: 0031815	Abnormal oral physiology	0/20
HP: 0031816	Abnormal oral morphology	0/20
HP: 0031826	Abnormal reflex	0/20
HP: 0031910	Abnormal cranial nerve physiology	0/20
HP: 0031983	Abnormal pulmonary thoracic imaging finding	0/20
HP: 0032039	Abnormality of the ocular adnexa	0/20
HP: 0032061	Hypereosinophilia	0/20
HP: 0032071	Pulmonary eosinophilic infiltration	0/20
HP: 0032101	Unusual infection	0/20
HP: 0032158	Unusual infection by anatomical site	0/20
HP: 0032159	Fungal meningitis	0/20
HP: 0032161	Coccidioidal meningitis	0/20
HP: 0032162	Unusual skin infection	0/20
HP: 0032169	Severe infection	0/20
HP: 0032172	Air crescent sign	0/20
HP: 0032249	Coccidioidomycosis	0/20
HP: 0032251	Abnormal immune system morphology	0/20
HP: 0032255	Opportunistic fungal infection	0/20
HP: 0032256	Histoplasmosis	0/20
HP: 0032309	Abnormal granulocyte count	0/20
HP: 0032516	Invasive dermatophyte infection	0/20
HP: 0040016	Prominent coccyx	0/20
HP: 0040017	Protruding coccyx	0/20
HP: 0040088	Abnormal lymphocyte count	0/20
HP: 0040090	Abnormality of the tympanic membrane	0/20
HP: 0040095	Neoplasm of the outer ear	0/20
HP: 0040096	Neoplasm of the inner ear	0/20
HP: 0040113	Old-aged sensorineural hearing impairment	0/20
HP: 0040115	Abnormality of the Eustachian tube	0/20
HP: 0040262	Glue ear	0/20
HP: 0040269	Blocked Eustachian tube	0/20
HP: 0040312	Temporomandibular arthritis	0/20
HP: 0045010	Abnormality of peripheral nerves	0/20
HP: 0045080	Decreased proportion of CD3-positive T cells	0/20
HP: 0100007	Neoplasm of the peripheral nervous system	0/20
HP: 0100256	Senile plaques	0/20
HP: 0100276	Skin pit	0/20
HP: 0100326	Immunologic hypersensitivity	0/20
HP: 0100547	Abnormality of forebrain morphology	0/20
HP: 0100662	Chondritis	0/20
HP: 0100703	Tongue thrusting	0/20
HP: 0100736	Abnormal soft palate morphology	0/20
HP: 0100763	Abnormality of the lymphatic system	0/20
HP: 0100765	Abnormality of the tonsils	0/20
HP: 0200034	Papule	0/20
HP: 0200149	CSF lymphocytic pleiocytosis	0/20
HP: 0410017	Otitis externa	0/20
HP: 0410042	Abnormal liver morphology	0/20
HP: 0500028	Cotton wool plaques	0/20