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 pattern (HP:0010720)

Parent Node:
Acquired abnormal hair pattern (HP:0011360)

..Starting node
..Tufted hairs (HP:0031283)

Term ID:

31283

Name:

Tufted hairs

Synonym:

Definition:

The presence of tufts of 8-15 hairs that appear to emerge from a single follicular orifice.

Comments:

Reference:

HP:0031283

Genes and Diseases:

Child Nodes:

Sister Nodes:

Early balding (HP:0002234)

Frontal balding (HP:0002292)

obsolete Alopecia areata (HP:0002229)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031283	HP:0031283	Tufted hairs	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.