Terminology Service for NFDI4Health

hereditary spherocytosis type 1

Go to external page http://purl.obolibrary.org/obo/DOID_0110916


A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of ANK1 on chromosome 8p11.21. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spherocytosis type 1

Synonyms
  • HS1
  • SPH1
  • hereditary spherocytosis 1
database cross reference
has obo namespace

disease_ontology

id

DOID:0110916