Disease #07181 (HMD (ddysplasia, mucoepithelial, hereditary), OMIM:158310)

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	HMD
Name	ddysplasia, mucoepithelial, hereditary
OMIM ID	158310
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SREBF1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-09-22 12:52:10 +02:00 (CEST)
Date last edited	N/A

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