hereditary spherocytosis type 2

Term ID

DOID:0110917

Synonyms

• hereditary spherocytosis 2
• HS2
• SPH2

Definition

A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTB gene on chromosome 14q23.3. https://www.ncbi.nlm.nih.gov/pubmed/8102379

References

• OMIM:616649

Ontology

Human Disease   ( DOID:0110917 )