Disease #05844 (OMOD1 (omodysplasia, type 1 (OMOD1)), OMIM:258315)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OMOD1
Name	omodysplasia, type 1 (OMOD1)
OMIM ID	258315
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GPC6
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-09-29 14:29:25 +02:00 (CEST)
Date last edited	N/A

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