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:
Constitutional symptom (HP:0025142)

Parent Node:
Body odor (HP:0500001)

..Starting node
..Musty odor (HP:0410021)

Term ID:

410021

Name:

Musty odor

Synonym:

Musty odor; Musty odour

Definition:

Pungent body odor.

Comments:

Reference:

HP:0410021

Genes and Diseases:

Child Nodes:

Sister Nodes:

Fish odor (HP:0410020)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0410021	HP:0410021	Musty odor	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.