Search Ontology:
Human Disease

hereditary spherocytosis type 3

Term ID
DOID:0110918
Synonyms
  • hereditary spherocytosis 3
  • HS3
  • SPH3
Definition
A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTA1 gene on chromosome 1q23.1. https://www.ncbi.nlm.nih.gov/pubmed/8941647
References
Ontology
Human Disease   ( DOID:0110918 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models