Disease #00120

To access more data, such as phenotypic and clinical characteristics of patients, contact us at canvas@rrp.demokritos.gr

CanVaS - A Greek Cancer Patient Genetic Variation Resource

LOVD v.3.0 Build 23 [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	FMNG
Name	Meningioma, familial, susceptibility to
OMIM ID	607174
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 2 genes	PTEN, SUFU
Associated tissues	-
Disease features	-
Remarks	-