Phenotype #0000027276

Individual ID 00033878
Associated disease CTRCT
Phenotype details microcornea; posterior polar progressing to dense nuclear/laminar, involvement anterior/posterior poles; congenital nystagmus
Diagnosis/Initial cataract
Inheritance Familial, autosomal dominant
Diagnosis/Definite CTRCT9
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Lars Hansen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Lars Hansen
Date created 2010-11-28 15:08:46 +01:00 (CET)
Date last edited 2023-03-19 17:36:13 +01:00 (CET)

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