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
..Post-partum hemorrhage (HP:0011891)

Term ID:

11891

Name:

Post-partum hemorrhage

Synonym:

Bleeding post-delivery; Post-partum haemorrhage

Definition:

Significant maternal haemorrhage/blood loss following deilvery of a child.

Comments:

Reference:

HP:0011891

Genes and Diseases:

Child Nodes:

Sister Nodes:

Prolonged bleeding after dental extraction (HP:0006298)

Prolonged bleeding after surgery (HP:0004846)

Prolonged bleeding following circumcision (HP:0030137)

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:0011891	HP:0011891	Post-partum hemorrhage	0	DIAPH1 CL E G H	1729	2876	OMIM:124900	Deafness, autosomal dominant 1		118
HP:0011891	HP:0011891	Post-partum hemorrhage	0	F10 CL E G H	2159	3528	ORPHA:328	Congenital factor X deficiency	HP:0040283 - Occasional	33
HP:0011891	HP:0011891	Post-partum hemorrhage	0	F13A1 CL E G H	2162	3531	ORPHA:331	Congenital factor XIII deficiency	HP:0040283 - Occasional	60
HP:0011891	HP:0011891	Post-partum hemorrhage	0	F13B CL E G H	2165	3534	ORPHA:331	Congenital factor XIII deficiency	HP:0040283 - Occasional	32
HP:0011891	HP:0011891	Post-partum hemorrhage	0	F2 CL E G H	2147	3535	ORPHA:325	Congenital factor II deficiency	HP:0040283 - Occasional	44
HP:0011891	HP:0011891	Post-partum hemorrhage	0	F5 CL E G H	2153	3542	ORPHA:326	Congenital factor V deficiency	HP:0040283 - Occasional	159
HP:0011891	HP:0011891	Post-partum hemorrhage	0	F7 CL E G H	2155	3544	ORPHA:327	Congenital factor VII deficiency	HP:0040283 - Occasional	70
HP:0011891	HP:0011891	Post-partum hemorrhage	0	F8 CL E G H	2157	3546	ORPHA:177926	Bleeding disorder in hemophilia A carriers without FVIII deficiency	HP:0040282 - Frequent	303
HP:0011891	HP:0011891	Post-partum hemorrhage	0	IKZF5 CL E G H	64376	14283	OMIM:619130	THROMBOCYTOPENIA 7; THC7
HP:0011891	HP:0011891	Post-partum hemorrhage	0	KIF23 CL E G H	9493	6392	ORPHA:98870	Congenital dyserythropoietic anemia type III	HP:0040283 - Occasional	1
HP:0011891	HP:0011891	Post-partum hemorrhage	0	RACGAP1 CL E G H	29127	9804	ORPHA:98870	Congenital dyserythropoietic anemia type III	HP:0040283 - Occasional
HP:0011891	HP:0011891	Post-partum hemorrhage	0	SERPINE1 CL E G H	5054	8583	ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency	HP:0040283 - Occasional	39

Genes (12) :DIAPH1 F10 F13A1 F13B F2 F5 F7 F8 IKZF5 KIF23 RACGAP1 SERPINE1

Diseases (10) :OMIM:124900 ORPHA:328 ORPHA:331 ORPHA:325 ORPHA:326 ORPHA:327 ORPHA:177926 OMIM:619130 ORPHA:98870 ORPHA:465

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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