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:
Strabismus (HP:0000486)

Parent Node:
Microtropia (HP:0031724)

..Starting node
..Microtropia with identity (HP:0031781)

Term ID:

31781

Name:

Microtropia with identity

Synonym:

Definition:

A type of microtropia with no manifest movement on cover test, the eccentric fixation point coinciding with the angle of ARC.

Comments:

Reference:

HP:0031781

Genes and Diseases:

Child Nodes:

Sister Nodes:

Microtropia without identity (HP:0031782)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031781	HP:0031781	Microtropia with identity	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.