Disease #05845 (OMOD2 (omodysplasia, type 2 (OMOD2)), OMIM:164745)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OMOD2
Name	omodysplasia, type 2 (OMOD2)
OMIM ID	164745
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FZD2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-09-29 14:30:16 +02:00 (CEST)
Date last edited	N/A

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