Disease #07191 (PMNDS (Parenti-Mignot neurodevelopmental syndrome), OMIM:619873)

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	PMNDS
Name	Parenti-Mignot neurodevelopmental syndrome
OMIM ID	619873
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CHD5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-10-01 12:17:43 +02:00 (CEST)
Date last edited	N/A

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