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 eyebrow morphology (HP:0000534)

Parent Node:
Broad eyebrow (HP:0011229)

..Starting node
..Extension of eyebrows towards upper eyelid (HP:0010731)

Term ID:

10731

Name:

Extension of eyebrows towards upper eyelid

Synonym:

Extension of eyebrows towards upper eyelid

Definition:

The eyebrows extend towards - or even all the way down to - the margin of the upper eyelid.

Comments:

Reference:

HP:0010731

Genes and Diseases:

Child Nodes:

Sister Nodes:

Broad lateral eyebrow (HP:0007933)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010731	HP:0010731	Extension of eyebrows towards upper eyelid	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.