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 sense of smell (HP:0004408)

Parent Node:
Hyposmia (HP:0004409)

..Starting node
..Partial hyposmia (HP:0010635)

Term ID:

10635

Name:

Partial hyposmia

Synonym:

Definition:

Reduced ability to perceive certain odorants (implies that the sense of smell is maintained for other classes of odorants).

Comments:

Reference:

HP:0010635

Genes and Diseases:

Child Nodes:

Sister Nodes:

Total hyposmia (HP:0010634)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010635	HP:0010635	Partial hyposmia	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.