primary autosomal recessive microcephaly 9

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Summary

Literature (0)

DOID:0070292 - primary autosomal recessive microcephaly 9

Disease Ontology Definition:A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21.

Synonyms: MCPH9,

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

: cep152

OMIM:

MIM:614852 - microcephaly 9, primary, autosomal recessive; mcph9

MIM:614852 - microcephaly 9, primary, autosomal recessive; mcph9

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

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

Parent(s): primary autosomal recessive microcephaly (is_a)