nonsyndromic aplasia cutis congenita

Term ID

DOID:0080661

Synonyms

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. (2)

References

• OMIM:107600

Ontology

Human Disease   ( DOID:0080661 )