Search Ontology:
Human Disease

hereditary spherocytosis type 4

Term ID
DOID:0110919
Synonyms
  • hereditary spherocytosis 4
  • HS4
  • SPH4
Definition
A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SLC4A1 gene on chromosome 17q21.31. https://www.ncbi.nlm.nih.gov/pubmed/7530501
References
Ontology
Human Disease   ( DOID:0110919 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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