Phenotype #0000277172

Individual ID 00383387
Associated disease CCTRCT
Phenotype details Two round-shaped opacifications in the middle of the lens
Diagnosis/Initial congenital cataract
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 14y (14 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2021-09-29 09:56:40 +02:00 (CEST)
Date last edited N/A

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