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hereditary spherocytosis type 2

Go to external page http://purl.obolibrary.org/obo/DOID_0110917

A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of SPTB on chromosome 14q23.3. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spherocytosis type 2

Synonyms
  • HS2
  • SPH2
  • hereditary spherocytosis 2
database cross reference
has obo namespace

disease_ontology

id

DOID:0110917