Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormality of blood and blood-forming tissues (HP:0001871)

Parent Node:
Abnormal bleeding (HP:0001892)

..Starting node
..Excessive bleeding from superficial cuts (HP:0030138)

Term ID:

30138

Name:

Excessive bleeding from superficial cuts

Synonym:

Excessive bleeding from superficial cuts

Definition:

An abnormally increased degree of bleeding following a superfical injury to the surface of the skin.

Comments:

Reference:

HP:0030138

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal onset of bleeding (HP:0040231)

Abnormal umbilical stump bleeding (HP:0011884)

Bleeding requiring red cell transfusion (HP:0011888)

Bleeding with minor or no trauma (HP:0011889)

Cephalohematoma (HP:0012541)

Epistaxis (HP:0000421)

Excessive bleeding after a venipuncture (HP:0030139)

Gingival bleeding (HP:0000225)

Internal hemorrhage (HP:0011029)

Menorrhagia (HP:0000132)

Oral cavity bleeding (HP:0030140)

Persistent bleeding after trauma (HP:0001934)

Prolonged bleeding following procedure (HP:0011890)

Prolonged bleeding time (HP:0003010)

Subcutaneous hemorrhage (HP:0001933)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030138	HP:0030138	Excessive bleeding from superficial cuts	0	EPHB2 CL E G H	2048	3393	OMIM:618462	Bleeding disorder, platelet-type, 22		7
HP:0030138	HP:0030138	Excessive bleeding from superficial cuts	0	F2 CL E G H	2147	3535	ORPHA:325	Congenital factor II deficiency	HP:0040283 - Occasional	44
HP:0030138	HP:0030138	Excessive bleeding from superficial cuts	0	ITGA2B CL E G H	3674	6138	OMIM:273800	Glanzmann thrombasthenia		69

Genes (3) :EPHB2 F2 ITGA2B

Diseases (3) :OMIM:618462 ORPHA:325 OMIM:273800

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