Summary Literature (0)

DOID:10907 - microcephaly

Disease Ontology Definition:A congenital nervous system abnormality that is characterized by a significantly smaller than normal head in infants.

Synonyms: Microcephalus, microencephaly

Xenbase Genes : mcph1, aspm, stil, dpp6, cpap, cdk5rap2, knl1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0001149 - microcephaly

MIM:

MIM:251200 - MICROCEPHALY 1, PRIMARY, AUTOSOMAL RECESSIVE; MCPH1

MIM:604321 - MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4

MIM:604804 - MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE; MCPH3

MIM:608393 - MICROCEPHALY 6, PRIMARY, AUTOSOMAL RECESSIVE; MCPH6

MIM:608716 - MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE; MCPH5

MIM:612703 - MICROCEPHALY 7, PRIMARY, AUTOSOMAL RECESSIVE; MCPH7

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

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