OBO ID: DOID:0110919
Term Name: hereditary spherocytosis type 4 Search Ontology:
Synonyms:
  • hereditary spherocytosis 4
  • HS4
  • SPH4
Definition: A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of SLC4A1 on chromosome 17q21.31. https://www.ncbi.nlm.nih.gov/pubmed/7530501
References:
Ontology: Human Disease   (DOID:0110919)
OTHER hereditary spherocytosis type 4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLC4A1 Spherocytosis, type 4 612653
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None