Phenotypes for disease #01050 (WS2E (Waardenburg syndrome, type 2E, with/without neurologic involvement (WS2E)), OMIM:611584)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000275377 Profound sensorineural hearing loss, Blue hypoplastic irides, Vestibular and semicircular canals dysplasia (mainly lateral and posterior), poorly characterized vestibular aqueduct. - - Familial, autosomal dominant - - - - - Karina Lezirovitz Mandelbaum 00381527
0000275378 iris heterochromia, white hair forelock and unilateral hearing loss - - Familial, autosomal dominant - - - - - Karina Lezirovitz Mandelbaum 00381528
0000308086 - hearing loss Waardenburg syndrome type 2E Isolated (sporadic) 00y02m? 00y08m? 00y02m? Hearing impairment - Ke Xu 00416319
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