Human Phenotype Ontology

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Hello! Guest! Please Login or Register! Clinician Mode

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:
Abnormal bleeding (HP:0001892)

Parent Node:
Prolonged bleeding following procedure (HP:0011890)

..Starting node
..Prolonged bleeding following circumcision (HP:0030137)

Term ID:

30137

Name:

Prolonged bleeding following circumcision

Synonym:

Prolonged bleeding following circumcision

Definition:

Bleeding that persists for a longer than usual time following circumcision.

Comments:

Reference:

HP:0030137

Genes and Diseases:

Child Nodes:

Sister Nodes:

Post-partum hemorrhage (HP:0011891)

Prolonged bleeding after dental extraction (HP:0006298)

Prolonged bleeding after surgery (HP:0004846)

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:0030137	HP:0030137	Prolonged bleeding following circumcision	0	F13A1 CL E G H	2162	3531	ORPHA:331	Congenital factor XIII deficiency	HP:0040283 - Occasional	60
HP:0030137	HP:0030137	Prolonged bleeding following circumcision	0	F13B CL E G H	2165	3534	ORPHA:331	Congenital factor XIII deficiency	HP:0040283 - Occasional	32
HP:0030137	HP:0030137	Prolonged bleeding following circumcision	0	F2 CL E G H	2147	3535	ORPHA:325	Congenital factor II deficiency	HP:0040283 - Occasional	44
HP:0030137	HP:0030137	Prolonged bleeding following circumcision	0	F5 CL E G H	2153	3542	ORPHA:326	Congenital factor V deficiency	HP:0040283 - Occasional	159
HP:0030137	HP:0030137	Prolonged bleeding following circumcision	0	F8 CL E G H	2157	3546	ORPHA:169802	Severe hemophilia A	HP:0040283 - Occasional	303
HP:0030137	HP:0030137	Prolonged bleeding following circumcision	0	FGA CL E G H	2243	3661	OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		47
HP:0030137	HP:0030137	Prolonged bleeding following circumcision	0	FGB CL E G H	2244	3662	OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		62
HP:0030137	HP:0030137	Prolonged bleeding following circumcision	0	FGG CL E G H	2266	3694	OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		34
HP:0030137	HP:0030137	Prolonged bleeding following circumcision	0	ITGA2B CL E G H	3674	6138	ORPHA:849	Glanzmann thrombasthenia	HP:0040282 - Frequent	69
HP:0030137	HP:0030137	Prolonged bleeding following circumcision	0	ITGB3 CL E G H	3690	6156	ORPHA:849	Glanzmann thrombasthenia	HP:0040282 - Frequent	80
HP:0030137	HP:0030137	Prolonged bleeding following circumcision	0	LMAN1 CL E G H	3998	6631	ORPHA:35909	Combined deficiency of factor V and factor VIII	HP:0040282 - Frequent	56
HP:0030137	HP:0030137	Prolonged bleeding following circumcision	0	MCFD2 CL E G H	90411	18451	ORPHA:35909	Combined deficiency of factor V and factor VIII	HP:0040282 - Frequent	77
HP:0030137	HP:0030137	Prolonged bleeding following circumcision	0	RBM8A CL E G H	9939	9905	OMIM:274000	Thrombocytopenia-absent radius syndrome		10

Genes (13) :F13A1 F13B F2 F5 F8 FGA FGB FGG ITGA2B ITGB3 LMAN1 MCFD2 RBM8A

Diseases (8) :ORPHA:331 ORPHA:325 ORPHA:326 ORPHA:169802 OMIM:202400 ORPHA:849 ORPHA:35909 OMIM:274000

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

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