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:
Phenotypic abnormality (HP:0000118)

Parent Node:
Constitutional symptom (HP:0025142)

..Starting node
..Chest tightness (HP:0031352)

Term ID:

31352

Name:

Chest tightness

Synonym:

Chest distress; Tightness in chest; Tightness of chest

Definition:

An unpleasant sensation of tightness or pressure in the chest.

Comments:

Reference:

HP:0031352

Genes and Diseases:

Child Nodes:

Sister Nodes:

Asthenia (HP:0025406)

Body odor (HP:0500001)

Chills (HP:0025143)

Fatigue (HP:0012378)

Hot flashes (HP:0031217)

Impairment of activities of daily living (HP:0031058)

Night sweats (HP:0030166)

Pain (HP:0012531)

Shivering (HP:0025144)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031352	HP:0031352	Chest tightness	0	DTNA CL E G H	1837	3057	OMIM:604169	Left ventricular noncompaction 1	163

Genes (1) :DTNA

Diseases (1) :OMIM:604169

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