Phenotype #0000027279

Individual ID 00033881
Associated disease CTRCT
Phenotype details congenital; nystagmus
Diagnosis/Initial cataract
Inheritance Familial, autosomal dominant
Diagnosis/Definite CTRCT9
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Lars Hansen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Lars Hansen
Date created 2007-06-21 20:00:00 +02:00 (CEST)
Date last edited 2023-03-19 17:33:10 +01:00 (CET)

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