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:
Abnormal oral cavity morphology (HP:0000163)

Parent Node:
Abnormal salivary gland morphology (HP:0010286)

..Starting node
..Sialadenitis (HP:0031281)

Term ID:

31281

Name:

Sialadenitis

Synonym:

Definition:

Inflammation of a salivary gland.

Comments:

Reference:

HP:0031281

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal parotid gland morphology (HP:0000197)

Abnormality of the sublingual glands (HP:0010288)

Abnormality of the submandibular glands (HP:0010287)

Ranula (HP:0030706)

Salivary gland neoplasm (HP:0100684)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031281	HP:0031281	Sialadenitis	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.