Human Gene Set: HP_ABNORMALITY_OF_THE_COMMON_COAGULATION_PATHWAY


Standard name HP_ABNORMALITY_OF_THE_COMMON_COAGULATION_PATHWAY
Systematic name M37722
Brief description Abnormality of the common coagulation pathway
Full description or abstract An abnormality of blood coagulation, common pathway. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0010990
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0010990
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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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