Search Ontology:
Human Disease

hereditary spherocytosis type 5

Term ID
DOID:0110920
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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