OBO ID: DOID:0080661
Term Name: nonsyndromic aplasia cutis congenita Search Ontology:
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 nonsyndromic aplasia cutis congenita PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
BMS1 ?Aplasia cutis congenita, nonsyndromic 107600
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.