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 uterus (HP:0000130)

Parent Node:
Abnormal uterus morphology (HP:0031105)

..Starting node
..Uterine synechiae (HP:0030712)

Term ID:

30712

Name:

Uterine synechiae

Synonym:

Asherman syndrome

Definition:

Adhesions or scar tissue that form inside the cavity of the uterus.

Comments:

Reference:

HP:0030712

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal endometrium morphology (HP:0030126)

Bicornuate uterus (HP:0000813)

Bifid uterus (HP:0000136)

Enlarged uterus (HP:0100878)

T-shaped uterus (HP:0031106)

Uterine neoplasm (HP:0010784)

Uterine prolapse (HP:0000139)

Uterine rupture (HP:0100718)

Uterus didelphys (HP:0003762)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030712	HP:0030712	Uterine synechiae	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.