Search Ontology:
Human Disease

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
Ontology
Human Disease   ( DOID:0110917 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models