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)

Parent Node:
Abnormal fallopian tube morphology (HP:0011027)

..Starting node
..Fallopian tube duplication (HP:0012885)

Term ID:

12885

Name:

Fallopian tube duplication

Synonym:

Accessory fallopian tube

Definition:

The presence of a supernumerary Fallopian tube.

Comments:

Reference:

HP:0012885

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aplasia/Hypoplasia of the fallopian tube (HP:0008655)

Fallopian tube cyst (HP:0012883)

Fallopian tube torsion (HP:0012884)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012885	HP:0012885	Fallopian tube duplication	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.