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:
Functional abnormality of the gastrointestinal tract (HP:0012719)

Parent Node:
Abnormal esophagus morphology (HP:0002031)

Parent Node:
Gastrointestinal obstruction (HP:0004796)

..Starting node
..Esophageal obstruction (HP:0005240)

Term ID:

5240

Name:

Esophageal obstruction

Synonym:

Definition:

Comments:

Reference:

HP:0005240

Genes and Diseases:

Child Nodes:

Sister Nodes:

Functional intestinal obstruction (HP:0005249)

Intestinal obstruction (HP:0005214)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005240	HP:0005240	Esophageal obstruction	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.