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:
Esodeviation (HP:0020045)

Parent Node:
Esotropia (HP:0000565)

..Starting node
..Non-accomodative esotropia (HP:0031760)

Term ID:

31760

Name:

Non-accomodative esotropia

Synonym:

Definition:

A form of esotropia in which the angle of deviation is not affected by accommodative effort.

Comments:

Reference:

HP:0031760

Genes and Diseases:

Child Nodes:

........

Near esotropia (HP:0031722)

........

Basic (constant) esotropia (HP:0031759)

........

Infantile (constant) esotropia (HP:0031761)

........

Distance esotropia (HP:0031762)

........

Cyclic esotropia (HP:0031763)

Sister Nodes:

Accommodative esotropia (HP:0020046)

Alternating esotropia (HP:0001137)

Consecutive esotropia (HP:0031767)

Secondary esotropia (HP:0031723)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031760	HP:0031760	Non-accomodative esotropia	0	CL E G H
HP:0031760	HP:0031761	Infantile constant esotropia	1	CL E G H
HP:0031760	HP:0031759	Basic constant esotropia	1	CL E G H
HP:0031760	HP:0031722	Near esotropia	1	CL E G H
HP:0031760	HP:0031763	Cyclic esotropia	1	CL E G H
HP:0031760	HP:0031762	Distance esotropia	1	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.