Phenotype #0000335764

Individual ID 00446562
Associated disease CTRCT
Phenotype details bilateral nuclear cataract; intraocular lens; no optic atrophy; no nystagmus; no esotropia
Diagnosis/Initial congenital catarct
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-01-17 21:03:04 +01:00 (CET)
Date last edited N/A

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