OBO ID: DOID:0111900
Term Name: autosomal dominant thrombophilia due to protein S deficiency Search Ontology:
Synonyms:
  • THPH5
Definition: A protein S deficiency characterized by reduced serum protein S levels and recurrent venous thrombosis that has_material_basis_in heterozygous mutation in the PROS1 gene on chromosome 3q11.1. (3)
References:
Ontology: Human Disease   ( DOID:0111900 )
OTHER autosomal dominant thrombophilia due to protein S deficiency PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PROS1 Thrombophilia 5 due to protein S deficiency, autosomal dominant 612336
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None