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

• OMIM:612690

Ontology

Human Disease   ( DOID:0110920 )