Phenotype #0000275379

Individual ID 00381529
Associated disease WS4C
Phenotype details Bilateral profound sensorineural hearing loss, iris heterochromia, chronic intestinal obstruction, congenital megacolon was suspected at birth not confirmed
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Karina Lezirovitz Mandelbaum
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Karina Lezirovitz Mandelbaum
Date created 2021-08-30 16:16:24 +02:00 (CEST)
Date last edited 2021-08-31 13:48:56 +02:00 (CEST)

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