Phenotype #0000324084

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	00433661
Associated disease	IHPRF1
Phenotype details	severe intellectual disability, developmental delay
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Marketa Wayhelova
Database submission license
Created by	Marketa Wayhelova
Date created	2023-03-12 19:42:24 +01:00 (CET)
Date last edited	2023-03-13 14:11:59 +01:00 (CET)

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