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 -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GLMN
Associated tissues -
Disease features autosomal dominant
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00163853 GVM-2 PubMed: Brouillard 2005 - - - - - - 0 - - GVM - GLMN GLMN 1 1 Pascal Brouillard
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