autosomal dominant microcephaly

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Summary

Literature (0)

DOID:14725 - autosomal dominant microcephaly

Disease Ontology Definition:A microcephaly that has_material_basis_in heterozygous mutation in an autosomal gene.

Synonyms:

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

: dpp6

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0007988 - autosomal dominant primary microcephaly

MONDO:0007988 - autosomal dominant primary microcephaly

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

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

Parent(s): autosomal dominant disease (is_a), microcephaly (is_a)