Moyamoya disease

Summary

DOID:13099 - Moyamoya disease

Disease Ontology Definition:A cerebral arterial disease characterized by constriction of certain arteries at the base of the brain. Blood flow is blocked by the constriction and also by blood clots.

Synonyms: progressive intracranial arterial occlusion

In OMIM:

OMIM:252350 - MOYAMOYA DISEASE 1; MYMY1
OMIM:300845 - MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM, AND FACIAL DYSMORPHISM; MYMY4
OMIM:607151 - MOYAMOYA DISEASE 2; MYMY2
OMIM:608796 - MOYAMOYA DISEASE 3; MYMY3
OMIM:614042 - MOYAMOYA DISEASE 5; MYMY5
OMIM:615750 - MOYAMOYA DISEASE 6 WITH OR WITHOUT ACHALASIA; MYMY6

OMIM:252350 - MOYAMOYA DISEASE 1; MYMY1

OMIM:300845 - MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM, AND FACIAL DYSMORPHISM; MYMY4

OMIM:607151 - MOYAMOYA DISEASE 2; MYMY2

OMIM:608796 - MOYAMOYA DISEASE 3; MYMY3

OMIM:614042 - MOYAMOYA DISEASE 5; MYMY5

OMIM:615750 - MOYAMOYA DISEASE 6 WITH OR WITHOUT ACHALASIA; MYMY6

In Mondo Disease Ontology:

MONDO:0016820 - Moyamoya disease

MONDO:0016820 - Moyamoya disease

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

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

: acta2, gucy1a1, rnf213

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

Parent(s): cerebral arterial disease (is_a)