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 gastrointestinal motility (HP:0030895)

Parent Node:
Abnormal gastrointestinal transit time (HP:0030896)

..Starting node
..Decreased intestinal transit time (HP:0030897)

Term ID:

30897

Name:

Decreased intestinal transit time

Synonym:

Definition:

A reduction in the length of time required for food to pass through the intestines.

Comments:

Reference:

HP:0030897

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030897	HP:0030897	Decreased intestinal transit time	0	ANO1 CL E G H	55107	21625	OMIM:620045
HP:0030897	HP:0030897	Decreased intestinal transit time	0	CLMP CL E G H	79827	24039	OMIM:615237	Congenital short bowel syndrome	.	7

Genes (2) :ANO1 CLMP

Diseases (2) :OMIM:620045 OMIM:615237

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.