Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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 without identity (HP:0031782)

Term ID:

31782

Name:

Microtropia without identity

Synonym:

Definition:

A type of microtropia in which the manifest movement is demonstrated on the cover-uncover test.

Comments:

Reference:

HP:0031782

Genes and Diseases:

Child Nodes:

Sister Nodes:

Microtropia with identity (HP:0031781)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031782	HP:0031782	Microtropia without 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.