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:
Exodeviation (HP:0020049)

Parent Node:
Exotropia (HP:0000577)

..Starting node
..Consecutive exotropia (HP:0031718)

Term ID:

31718

Name:

Consecutive exotropia

Synonym:

Definition:

Exotropia in an individual who has previously had esotropia or esophoria.

Comments:

Reference:

HP:0031718

Genes and Diseases:

Child Nodes:

Sister Nodes:

Alternating exotropia (HP:0031717)

Constant exotropia (HP:0031713)

Cyclic exotropia (HP:0031716)

Distance exotropia (HP:0031714)

Near exotropia (HP:0031715)

obsolete Congenital exotropia (HP:0008033)

Sensory exotropia (HP:0031721)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031718	HP:0031718	Consecutive exotropia	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.