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:
Abnormality of the tongue (HP:0000157)

Parent Node:
Abnormal tongue physiology (HP:0030810)

..Starting node
..Tongue pain (HP:0030811)

Term ID:

30811

Name:

Tongue pain

Synonym:

Painful tongue

Definition:

An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the tongue.

Comments:

Reference:

HP:0030811

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormality of taste sensation (HP:0000223)

Movement abnormality of the tongue (HP:0000182)

Tongue fasciculations (HP:0001308)

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:0030811	HP:0030811	Tongue pain	0	NTRK1 CL E G H	4914	8031	ORPHA:642	Hereditary sensory and autonomic neuropathy type 4	HP:0040283 - Occasional	97

Genes (1) :NTRK1

Diseases (1) :ORPHA:642

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