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
..obsolete Pointed frontal hairline (HP:0004544)

Term ID:

4544

Name:

obsolete Pointed frontal hairline

Synonym:

Definition:

Comments:

Reference:

HP:0004544

Genes and Diseases:

Child Nodes:

Sister Nodes:

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

High anterior hairline (HP:0009890)

Low anterior hairline (HP:0000294)

Sparse anterior scalp hair (HP:0004768)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004544	HP:0004544	obsolete Pointed frontal hairline	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.