Phenotype #0000053431

Individual ID 00065092
Associated disease CCTRCT
Phenotype details congenital cataract (HP:0000519), corneal opacity (HP:0007957), anterior segment dysgenesis (HP:0007700)
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Deepti Anand
Database submission license No license selected
Created by Johan den Dunnen
Date created 2016-06-18 10:36:00 +02:00 (CEST)
Date last edited N/A

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