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 ovarian morphology (HP:0031065)

Parent Node:
Ovarian cyst (HP:0000138)

..Starting node
..Hemorrhagic ovarian cyst (HP:0012886)

Term ID:

12886

Name:

Hemorrhagic ovarian cyst

Synonym:

Definition:

An abdominal mass formed by bleeding into a follicular ovarian cyst or corpus luteum cyst.

Comments:

Reference:

HP:0012886

Genes and Diseases:

Child Nodes:

Sister Nodes:

Calcified ovarian cyst (HP:0030425)

Ovarian dermoid cyst (HP:0025274)

Ovarian serous cystadenoma (HP:0012887)

Polycystic ovaries (HP:0000147)

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:0012886	HP:0012886	Hemorrhagic ovarian cyst	0	FSHR CL E G H	2492	3969	ORPHA:64739	Ovarian hyperstimulation syndrome	HP:0040282 - Frequent	50
HP:0012886	HP:0012886	Hemorrhagic ovarian cyst	0	PRLR CL E G H	5618	9446	ORPHA:397685	Familial hyperprolactinemia	HP:0040282 - Frequent	2

Genes (2) :FSHR PRLR

Diseases (2) :ORPHA:64739 ORPHA:397685

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