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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Abnormal onset of bleeding (HP:0040231)help
Term ID: 40231
Name: Abnormal onset of bleeding
Synonym:
Definition:
Comments:
Reference: HP:0040231
Genes and Diseases:
 
       Child Nodes:
........expandDelayed onset bleeding (HP:0040232) help

 Sister Nodes: 
..expandAbnormal umbilical stump bleeding (HP:0011884) help
..expandBleeding requiring red cell transfusion (HP:0011888) help
..expandBleeding with minor or no trauma (HP:0011889) 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:0040231HP:0040231Abnormal onset of bleeding0F13A1 CL E G H21623531ORPHA:331Congenital factor XIII deficiency60
HP:0040231HP:0040231Abnormal onset of bleeding0F13B CL E G H21653534ORPHA:331Congenital factor XIII deficiency32
HP:0040231HP:0040232Delayed onset bleeding1F13A1 CL E G H21623531ORPHA:331Congenital factor XIII deficiencyHP:0040283 - Occasional60
HP:0040231HP:0040232Delayed onset bleeding1F13B CL E G H21653534ORPHA:331Congenital factor XIII deficiencyHP:0040283 - Occasional32


Genes (2) :F13A1 F13B

Diseases (1) :ORPHA:331
 

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