OBO ID: DOID:0110920
Term Name: hereditary spherocytosis type 5 Search Ontology:
Synonyms:
  • hereditary spherocytosis 5
  • HS5
  • SPH5
Definition: A hereditary spherocytosis that has_material_basis_in a mutation of the EPB42 gene on chromosome 15q15.2. https://www.ncbi.nlm.nih.gov/pubmed/1558976
References:
Ontology: Human Disease   ( DOID:0110920 )
OTHER hereditary spherocytosis type 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
EPB42 Spherocytosis, type 5
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None