OBO ID: DOID:0111846
Term Name: X-linked congenital hemolytic anemia Search Ontology:
Synonyms:
Definition: A congenital hemolytic anemia characterized by mild congenital hemolytic anemia without morphologic red cell abnormalities that has_material_basis_in hemizygous mutation in the ATP11C gene on chromosome Xq27.1. https://www.ncbi.nlm.nih.gov/pubmed/26944472
References:
Ontology: Human Disease   ( DOID:0111846 )
OTHER X-linked congenital hemolytic anemia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ATP11C ?Hemolytic anemia, congenital, X-linked 301015
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None