Disease #01349 (GVM (malformations, glomuvenous (GVM)), OMIM:138000)

Official abbreviation GVM
Name malformations, glomuvenous (GVM)
OMIM ID 138000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene GLMN
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00163853 GVM-2 PubMed: Brouillard 2005 - - - - - - - - - GVM - GLMN GLMN 1 1 Pascal Brouillard
00464065 - - - M - - - - - - - GVM - GLMN GLMN 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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