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DOID:0080690 - RASopathy
Disease Ontology Definition:A syndrome that has_material_basis_in mutations in genes that alter the Ras subfamily and mitogen-activated protein kinases that control signal transduction.
Synonyms: RAS/mitogen-activated protein kinase syndrome
Xenbase Genes
:
map2k1,
hras,
rasa2,
spred1,
nf1,
mras,
shoc2,
smarcb1,
ppp1cb,
msh2,
nf2,
lztr1,
sos2,
sos1,
braf,
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
syndrome (is_a)