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)

Grandparent Node:
Abnormality of the curvature of the cornea (HP:0100691)

Parent Node:
Astigmatism (HP:0000483)

..Starting node
..Lenticular astigmatism (HP:0031791)

Term ID:

31791

Name:

Lenticular astigmatism

Synonym:

Definition:

A type of astigmatism related to an irregular shape of the lens.

Comments:

Reference:

HP:0031791

Genes and Diseases:

Child Nodes:

Sister Nodes:

Against the rule astigmatism (HP:0031789)

Corneal astigmatism (HP:0025612)

Hyperopic astigmatism (HP:0000484)

Irregular astigmatism (HP:0031792)

Mixed astigmatism (HP:0031790)

Myopic astigmatism (HP:0500041)

Oblique astigmatism (HP:0031787)

With the rule astigmatism (HP:0031788)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031791	HP:0031791	Lenticular astigmatism	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.