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:
Abnormal morphology of female internal genitalia (HP:0000008)

Grandparent Node:
Irregular menstruation (HP:0000858)

Parent Node:
Abnormality of the menstrual cycle (HP:0000140)

..Starting node
..Polymenorrhea (HP:0400007)

Term ID:

400007

Name:

Polymenorrhea

Synonym:

Definition:

Frequent menses; menstrual cycles lasting less than 21 days.

Comments:

Reference:

HP:0400007

Genes and Diseases:

Child Nodes:

Sister Nodes:

Amenorrhea (HP:0000141)

Delayed menarche (HP:0012569)

Menometrorrhagia (HP:0400008)

Menorrhagia (HP:0000132)

Metrorrhagia (HP:0100608)

Oligomenorrhea (HP:0000876)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0400007	HP:0400007	Polymenorrhea	0	CL E G H

Genes (0) :

Diseases (0) :

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