Phenotype #0000275382

Individual ID 00381532
Associated disease WS2A
Phenotype details profound sensorineural hearing loss, Hypoplastic irides at birth that turned out into partial
heterochromia irides after few months
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 16:46:46 +02:00 (CEST)
Date last edited 2021-08-31 13:53:22 +02:00 (CEST)

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