Search Ontology:
Human Disease

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
Ontology
Human Disease   ( DOID:0080661 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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