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 abdominal organs (HP:0002012)

Parent Node:
Abnormality of the peritoneum (HP:0002585)

..Starting node
..Peritoneal effusion (HP:0030995)

Term ID:

30995

Name:

Peritoneal effusion

Synonym:

Definition:

An increase in the amount of fluid present in the peritoneal cavity (between the layers of the peritoneum that lines the abdomen).

Comments:

Reference:

HP:0030995

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hemoperitoneum (HP:0011854)

Peritoneal abscess (HP:0100592)

Peritoneal mesothelioma (HP:0100003)

Peritonitis (HP:0002586)

Retroperitoneal fibrosis (HP:0005200)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030995	HP:0030995	Peritoneal effusion	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.