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:
Inflammation of the large intestine (HP:0002037)

Parent Node:
Colitis (HP:0002583)

..Starting node
..Acute colitis (HP:0100282)

Term ID:

100282

Name:

Acute colitis

Synonym:

Definition:

An acute and self-limited inflammatory disease of the large intestine (colon, cecum and rectum).

Comments:

Reference:

HP:0100282

Genes and Diseases:

Child Nodes:

........

Enterocolitis (HP:0004387)

Sister Nodes:

Chronic colitis (HP:0100281)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100282	HP:0100282	Acute colitis	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.