Phenotype #0000324405

Individual ID 00434026
Associated disease CTRCT
Phenotype details congenital hereditary nuclear cataract; microphthalmos, concomitant strabismus, nystagmus; visual acuity 0.2/0.4
Diagnosis/Initial cataract
Inheritance Familial, autosomal dominant
Diagnosis/Definite CTRCT2
Age/Examination -
Age/Diagnosis 1m
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 2023-03-17 16:18:55 +01:00 (CET)
Date last edited N/A

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