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 the ovary (HP:0000137)

Parent Node:
Abnormal ovarian morphology (HP:0031065)

..Starting node
..Ectopic ovary (HP:0031086)

Term ID:

31086

Name:

Ectopic ovary

Synonym:

Undescended ovary

Definition:

Undescended or ectopic ovaries are characterized by the attachment of the upper pole of the ovary to an area above the level of the common iliac vessels.

Comments:

Reference:

HP:0031086

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aplasia/Hypoplasia of the ovary (HP:0010462)

Enlarged ovaries (HP:0100879)

Oophoritis (HP:0031259)

Ovarian cyst (HP:0000138)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031086	HP:0031086	Ectopic ovary	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.

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