Phenotypes for disease #01049 (WS4C (Waardenburg syndrome, type 4C (WS4C)), OMIM:613266)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000274569 - - - Unknown - - - - - Karina Lezirovitz Mandelbaum 00380716
0000275379 Bilateral profound sensorineural hearing loss, iris heterochromia, chronic intestinal obstruction, congenital megacolon was suspected at birth not confirmed - - Isolated (sporadic) - - - - - Karina Lezirovitz Mandelbaum 00381529
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