Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the coagulation cascade (HP:0003256)help
Parent Node:
expandAbnormality of prothrombin (HP:0012200)help
..Starting node
..expandReduced prothrombin consumption (HP:0003337)help
Term ID: 3337
Name: Reduced prothrombin consumption
Synonym: Poor prothrombin consumption
Definition: The prothrombin consumption test measures the formation of intrinsic thromboplastin by determining the residual serum prothrombin after blood clotting is complete. If there is a defect in the process, less prothrombin will be converted to thrombin than normal (less prothrombin is consumed). This test may be abnormal with conditions including deficiency of factors VIII or IX, with circulating anticoagulants, thrombocytopenia.
Comments:
Reference: HP:0003337
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandobsolete Reduced prothrombin activity (HP:0012201) help
..expandProlonged prothrombin time (HP:0008151) help
..expandReduced prothrombin antigen (HP:0040250) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0003337HP:0003337Reduced prothrombin consumption0GFI1B CL E G H83284238OMIM:187900Bleeding disorder, platelet-type, 17.3


Genes (1) :GFI1B

Diseases (1) :OMIM:187900
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.