Term Name:	nonsyndromic aplasia cutis congenita
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.
Ontology:	Human Disease [DOID:0080661]   ( DOID:0080661 )