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:
Aplasia/Hypoplasia of the vagina (HP:0011026)

Parent Node:
Aplasia of the vagina (HP:0003250)

..Starting node
..Aplasia of the lower vagina (HP:0012674)

Term ID:

12674

Name:

Aplasia of the lower vagina

Synonym:

Absent lower vagina; Agenesis of the lower vagina

Definition:

A failure to develop of the lower part of the vagina.

Comments:

Reference:

HP:0012674

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aplasia of the upper vagina (HP:0012673)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012674	HP:0012674	Aplasia of the lower vagina	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.