Terminology Service for NFDI4Health

hereditary spherocytosis type 4

Go to external page http://purl.obolibrary.org/obo/DOID_0110919


A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of SLC4A1 on chromosome 17q21.31. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spherocytosis type 4

Synonyms
  • HS4
  • SPH4
  • hereditary spherocytosis 4
database cross reference
has obo namespace

disease_ontology

id

DOID:0110919