Search Ontology:
Human Disease

hereditary spherocytosis type 1

Term ID
DOID:0110916
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 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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