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 eyelid morphology (HP:0000492)

Parent Node:
Epicanthus (HP:0000286)

..Starting node
..Epicanthus tarsalis (HP:0031771)

Term ID:

31771

Name:

Epicanthus tarsalis

Synonym:

Definition:

A type of epicanthus in which a primarily upper lid fold is present.

Comments:

Reference:

HP:0031771

Genes and Diseases:

Child Nodes:

Sister Nodes:

Epicanthus inversus (HP:0000537)

Epicanthus palpebralis (HP:0031770)

Epicanthus superciliaris (HP:0025611)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031771	HP:0031771	Epicanthus tarsalis	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.