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 refraction (HP:0000539)

Parent Node:
Myopia (HP:0000545)

..Starting node
..Latent myopia (HP:0500066)

Term ID:

500066

Name:

Latent myopia

Synonym:

Definition:

The difference between total and manifest myopia.

Comments:

Reference:

HP:0500066

Genes and Diseases:

Child Nodes:

Sister Nodes:

Axial myopia (HP:0031730)

High myopia (HP:0011003)

Mild myopia (HP:0025573)

Moderate myopia (HP:0031624)

obsolete Congenital myopia (HP:0008012)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0500066	HP:0500066	Latent myopia	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.