Disease #07228 (NEDDFAC (nurodevelopmental disorder with dysmorphic facies and thin corpus callosum), OMIM:619480)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	NEDDFAC
Name	nurodevelopmental disorder with dysmorphic facies and thin corpus callosum
OMIM ID	619480
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SUPT16H
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-02-02 14:22:17 +01:00 (CET)
Date last edited	N/A

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