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Summary Literature (7)
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

Referenced OMIM:
OMIM:251200 - MICROCEPHALY 1, PRIMARY, AUTOSOMAL RECESSIVE; MCPH1
OMIM:604321 - MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4
OMIM:604804 - MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE; MCPH3
OMIM:608393 - MICROCEPHALY 6, PRIMARY, AUTOSOMAL RECESSIVE; MCPH6
OMIM:608716 - MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE; MCPH5
OMIM:612703 - MICROCEPHALY 7, PRIMARY, AUTOSOMAL RECESSIVE; MCPH7

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

Xenbase Genes : mcph1, aspm, stil, cenpj, cdk5rap2, knl1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): congenital nervous system abnormality (is_a)


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