OBO ID: DOID:0110916
Term Name: hereditary spherocytosis type 1 Search Ontology:
Synonyms:
  • hereditary spherocytosis 1
  • HS1
  • SPH1
Definition: A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the ANK1 gene on chromosome 8p11.21. https://www.ncbi.nlm.nih.gov/pubmed/2675425
References:
Ontology: Human Disease   ( DOID:0110916 )
OTHER hereditary spherocytosis type 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ANK1 Spherocytosis, type 1 182900
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None