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 hair morphology (HP:0001595)

Grandparent Node:
Abnormal scalp morphology (HP:0001965)

Parent Node:
Abnormality of the nose (HP:0000366)

Parent Node:
Abnormality of the scalp hair (HP:0100037)

..Starting node
..Abnormality of nasal hair (HP:0040057)

Term ID:

40057

Name:

Abnormality of nasal hair

Synonym:

Abnormality of nasal hair; Abnormality of nose hair

Definition:

Comments:

Reference:

HP:0040057

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormality of the hairline (HP:0009553)

Alopecia of scalp (HP:0002293)

Slow-growing scalp hair (HP:0100038)

Sparse scalp hair (HP:0002209)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040057	HP:0040057	Abnormality of nasal hair	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.