nonsyndromic aplasia cutis congenita

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Summary

Literature (0)

DOID:0080661 - nonsyndromic aplasia cutis congenita

Disease Ontology Definition:A skin disease characterized by localized areas of missing skin that resemble ulcers or oopen wounds in new borns and that has_material_basis_in heterozygous mutation in the BMS1 gene on chromosome 10q11.

Synonyms: nonsyndromic aplasia cutis congenita

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

: bms1

MIM:

MIM:107600 - APLASIA CUTIS CONGENITA, NONSYNDROMIC; ACC

MIM:107600 - APLASIA CUTIS CONGENITA, NONSYNDROMIC; ACC

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

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

Parent(s): skin disease (is_a)