cerebral cavernous malformation 3

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Summary

Literature (0)

DOID:0060671 - cerebral cavernous malformation 3

Disease Ontology Definition:A cerebral cavernous malformation that has_material_basis_in mutation in the PDCD10 gene on chromosome 3q26.1.

Synonyms: CCM3

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: pdcd10

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011305 - cerebral cavernous malformation 3

MONDO:0011305 - cerebral cavernous malformation 3

MIM:

MIM:603285 - CEREBRAL CAVERNOUS MALFORMATIONS 3; CCM3

MIM:603285 - CEREBRAL CAVERNOUS MALFORMATIONS 3; CCM3

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): cerebral cavernous malformation (is_a)