Disease #07143 (NEDGFC (neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities), OMIM:620113)

Global Variome shared LOVD

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Official abbreviation	NEDGFC
Name	neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities
OMIM ID	620113
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FRA10AC1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-12-18 19:30:30 +01:00 (CET)
Date last edited	N/A

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