Phenotype #0000353717

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00468563
Associated disease	ASGD2
Phenotype details	see paper; ..., primary aphakia, bilateral congenital corneal opacity, glaucoma; iridocorneal adhesion
Diagnosis/Initial	ocular anterior segment disease
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	ASGD2
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2025-11-10 19:03:47 +01:00 (CET)
Date last edited	N/A

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