OBO ID: DOID:0110917
Term Name: hereditary spherocytosis type 2 Search Ontology:
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 hereditary spherocytosis type 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SPTB Spherocytosis, type 2 616649
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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