Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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 ovarian morphology (HP:0031065)

Parent Node:
Ovarian cyst (HP:0000138)

..Starting node
..Calcified ovarian cyst (HP:0030425)

Term ID:

30425

Name:

Calcified ovarian cyst

Synonym:

Definition:

A cyst of the ovary that exhibits deposition of calcium salts.

Comments:

Reference:

HP:0030425

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hemorrhagic ovarian cyst (HP:0012886)

Ovarian dermoid cyst (HP:0025274)

Ovarian serous cystadenoma (HP:0012887)

Polycystic ovaries (HP:0000147)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030425	HP:0030425	Calcified ovarian cyst	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.