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 forehead (HP:0000290)

Grandparent Node:
Abnormality of the hairline (HP:0009553)

Parent Node:
Abnormality of the frontal hairline (HP:0000599)

..Starting node
..Extension of hair growth on temples to lateral eyebrow (HP:0005325)

Term ID:

5325

Name:

Extension of hair growth on temples to lateral eyebrow

Synonym:

Unusual hairline with hair growth on temples extending to lateral eyebrow

Definition:

A pattern of hair growth in which there is hair extending from the temples to the lateral eyebrows.

Comments:

Reference:

HP:0005325

Genes and Diseases:

Child Nodes:

Sister Nodes:

High anterior hairline (HP:0009890)

Low anterior hairline (HP:0000294)

obsolete Pointed frontal hairline (HP:0004544)

Sparse anterior scalp hair (HP:0004768)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005325	HP:0005325	Extension of hair growth on temples to lateral eyebrow	0	CPOX CL E G H	1371	2321	ORPHA:79273	Hereditary coproporphyria	HP:0040283 - Occasional	72
HP:0005325	HP:0005325	Extension of hair growth on temples to lateral eyebrow	0	FRAS1 CL E G H	80144	19185	OMIM:219000	Fraser syndrome	.	353

Genes (2) :CPOX FRAS1

Diseases (2) :ORPHA:79273 OMIM:219000

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.