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 eyelash morphology (HP:0000499)

Parent Node:
Abnormality of upper eyelashes (HP:0040051)

Parent Node:
Long eyelashes (HP:0000527)

..Starting node
..Long upper eyelashes (HP:0007840)

Term ID:

7840

Name:

Long upper eyelashes

Synonym:

Ciliary trichomegaly of upper eyelashes; Increased length of upper eyelashes; Long upper eyelashes

Definition:

Increased length of the upper eyelashes.

Comments:

Reference:

HP:0007840

Genes and Diseases:

Child Nodes:

Sister Nodes:

Long eyelashes in irregular rows (HP:0007740)

Long lower eyelashes (HP:0040053)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007840	HP:0007840	Long upper eyelashes	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.