Human Phenotype Ontology 
Grandparent Node:
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Abnormality of blood and blood-forming tissues (HP:0001871)help
Parent Node:
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Abnormal bleeding (HP:0001892)help
..Starting node
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Bleeding with minor or no trauma (HP:0011889)help
Term ID: 11889
Name: Bleeding with minor or no trauma
Synonym: Bleeding with minor or no trauma; Easy bleeding
Definition: Significant bleeding or hemorrhage without significant precipitating factor.
Comments:
Reference: HP:0011889
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal onset of bleeding (HP:0040231) help
..expandAbnormal umbilical stump bleeding (HP:0011884) help
..expandBleeding requiring red cell transfusion (HP:0011888) help
..expandCephalohematoma (HP:0012541) help
..expandEpistaxis (HP:0000421) help
..expandExcessive bleeding after a venipuncture (HP:0030139) help
..expandExcessive bleeding from superficial cuts (HP:0030138) help
..expandGingival bleeding (HP:0000225) help
..expandInternal hemorrhage (HP:0011029) help
..expandMenorrhagia (HP:0000132) help
..expandOral cavity bleeding (HP:0030140) help
..expandPersistent bleeding after trauma (HP:0001934) help
..expandProlonged bleeding following procedure (HP:0011890) help
..expandProlonged bleeding time (HP:0003010) help
..expandSubcutaneous hemorrhage (HP:0001933) 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:0011889HP:0011889Bleeding with minor or no trauma0F13A1 CL E G H21623531ORPHA:331Congenital factor XIII deficiencyHP:0040283 - Occasional60
HP:0011889HP:0011889Bleeding with minor or no trauma0F13B CL E G H21653534ORPHA:331Congenital factor XIII deficiencyHP:0040283 - Occasional32
HP:0011889HP:0011889Bleeding with minor or no trauma0F8 CL E G H21573546ORPHA:169805Moderate hemophilia AHP:0040282 - Frequent303
HP:0011889HP:0011889Bleeding with minor or no trauma0KRT1 CL E G H38486412ORPHA:79503Ichthyosis hystrix of Curth-MacklinHP:0040283 - Occasional100
HP:0011889HP:0011889Bleeding with minor or no trauma0LMAN1 CL E G H39986631ORPHA:35909Combined deficiency of factor V and factor VIIIHP:0040282 - Frequent56
HP:0011889HP:0011889Bleeding with minor or no trauma0MCFD2 CL E G H9041118451ORPHA:35909Combined deficiency of factor V and factor VIIIHP:0040282 - Frequent77
HP:0011889HP:0011889Bleeding with minor or no trauma0SLC37A4 CL E G H25424061OMIM:619525CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIw; CDG2W110


Genes (7) :F13A1 F13B F8 KRT1 LMAN1 MCFD2 SLC37A4

Diseases (5) :ORPHA:331 ORPHA:169805 ORPHA:79503 ORPHA:35909 OMIM:619525
 

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