Human Gene Set: HP_ABNORMALITY_OF_PROTHROMBIN


Standard name HP_ABNORMALITY_OF_PROTHROMBIN
Systematic name M38041
Brief description Abnormality of prothrombin
Full description or abstract An anomaly of clotting factor II, which is known as prothrombin, a vitamin K-dependent proenzyme that functions in the blood coagulation cascade. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0012200
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0012200
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
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Version history 2025.1.Hs: Updated to HPO Release 2025-05-06.

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