Disease #02638 (meningioma (meningioma, familial, susceptibility to), OMIM:607174)

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Official abbreviation	meningioma
Name	meningioma, familial, susceptibility to
OMIM ID	607174
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 6 genes	MN1, NF2, PDGFB, PTEN, SMARCE1, SUFU
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A