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:
Esotropia (HP:0000565)

Parent Node:
Non-accomodative esotropia (HP:0031760)

..Starting node
..Basic constant esotropia (HP:0031759)

Term ID:

31759

Name:

Basic constant esotropia

Synonym:

Basic (constant) esotropia

Definition:

A form of convergent strabismus (esotropia) in which the deviation is present under all conditions (ie at all distances and at all times).

Comments:

Reference:

HP:0031759

Genes and Diseases:

Child Nodes:

Sister Nodes:

Cyclic esotropia (HP:0031763)

Distance esotropia (HP:0031762)

Infantile constant esotropia (HP:0031761)

Near esotropia (HP:0031722)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031759	HP:0031759	Basic constant esotropia	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.