Phenotype #0000252292

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00334107
Associated disease	-
Phenotype details	clinical category IB8
Diagnosis/Initial	syndromic retinitis pigmentosa (Heimler syndrome)
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	14y (14 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Johan den Dunnen
Date created	2021-02-26 16:26:23 +01:00 (CET)
Date last edited	N/A

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