Phenotype #0000324522

Individual ID 00434164
Associated disease CTRCT
Phenotype details lamellar cataract; no microphthalmia; no microcornea; no iris malformations
Diagnosis/Initial cataract
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 2023-03-21 17:22:01 +01:00 (CET)
Date last edited N/A

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