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,

Echinobase Genes : aspm, stil


OMIM:

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: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

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