Phenotype #0000334172

Individual ID 00444922
Associated disease CTRCT
Phenotype details see paper; ..., bilateral cataract, umbilical hernia; father cataract, glaucoma, umbilical hernia, bilateral iridectomies with iris cysts, 40y-visual acuity R 6/18 L 6/12, HCD 11 bilateral
Diagnosis/Initial cataract
Inheritance Familial, autosomal dominant
Diagnosis/Definite CTRCT22
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 2023-12-28 19:27:56 +01:00 (CET)
Date last edited N/A

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