Disease #07016 (NCFD (neurocardiofaciodigital syndrome), OMIM:619869)

Global Variome shared LOVD

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

Official abbreviation	NCFD
Name	neurocardiofaciodigital syndrome
OMIM ID	619869
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MAPKAPK5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-07-24 14:33:37 +02:00 (CEST)
Date last edited	N/A

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