Disease #00313 (DESMD (desmoid disease, hereditary), OMIM:135290)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Johan den Dunnen

Official abbreviation	DESMD
Name	desmoid disease, hereditary
OMIM ID	135290
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	APC
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-01-27 14:57:06 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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