Disease #05953 (PMGEDSV (polymicrogyria, with/without vascular-type EDS), OMIM:618343)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	PMGEDSV
Name	polymicrogyria, with/without vascular-type EDS
OMIM ID	618343
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	COL3A1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-07-21 14:04:34 +02:00 (CEST)
Date last edited	N/A

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