FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term nonsyndromic aplasia cutis congenita ID (Ontology) DOID:0080661 (Human Disease)
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.
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 Genes
 nonsyndromic aplasia cutis congenita       1
 for disease ribbon | nonsyndromic aplasia cutis congenita       1
 model of | nonsyndromic aplasia cutis congenita       1
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  integumentary system disease
   |__skin disease
       |__nonsyndromic aplasia cutis congenita  1 rec.
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MIM:107600