Phenotype #0000333394

Individual ID 00444140
Associated disease CTRCT
Phenotype details see paper; ..., microcornea, cataract/aphakia, optic disc and macular coloboma, nystagmus, blepharoptosis
Diagnosis/Initial cataracts
Inheritance Familial, autosomal dominant
Diagnosis/Definite CTRCT9
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 2023-12-18 20:45:44 +01:00 (CET)
Date last edited N/A

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