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 intestine morphology (HP:0002242)

Parent Node:
Intestinal perforation (HP:0031368)

..Starting node
..Rectal perforation (HP:0031371)

Term ID:

31371

Name:

Rectal perforation

Synonym:

Definition:

A hole (perforation) in the wall of the rectum.

Comments:

Reference:

HP:0031371

Genes and Diseases:

Child Nodes:

Sister Nodes:

Colon perforation (HP:0031369)

Small intestinal perforation (HP:0031370)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031371	HP:0031371	Rectal perforation	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.