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 physiology (HP:0031066)

..Starting node
..Empty ovarian follicle (HP:0031067)

Term ID:

31067

Name:

Empty ovarian follicle

Synonym:

Empty follicle syndrome

Definition:

A failure to collect oocytes after an apparently normal controlled ovarian hyperstimulation cycle for in vitro fertilization.

Comments:

Reference:

HP:0031067

Genes and Diseases:

Child Nodes:

Sister Nodes:

Female hypogonadism (HP:0000134)

Premature ovarian insufficiency (HP:0008209)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031067	HP:0031067	Empty ovarian follicle	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.