Phenotypes for disease #01605 (WS2A (Waardenburg syndrome, type 2A (WS2A)), OMIM:193510)

6 entries on 1 page. Showing entries 1 - 6.
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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     
0000060257 - - - Familial, autosomal dominant - - - - - Celia Zazo-Seco 00037766
0000251618 - - - Familial, autosomal dominant - - - - - Ehsan Razmara 00333431
0000274565 - - - Isolated (sporadic) - - - - - Karina Lezirovitz Mandelbaum 00380712
0000274954 Bilateral profound SHL (cochlear implanted - different service), iris heterochromia and blonde hair backlock - - Familial, autosomal dominant - - - - - Karina Lezirovitz Mandelbaum 00381103
0000274955 blonde hair lock behind the ear, normal hearing - - Familial, autosomal dominant - - - - - Karina Lezirovitz Mandelbaum 00381104
0000275382 profound sensorineural hearing loss, Hypoplastic irides at birth that turned out into partial heterochromia irides after few months - - Isolated (sporadic) - - - - - Karina Lezirovitz Mandelbaum 00381532
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