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:
Incomitant strabismus (HP:0025068)

..Starting node
..Double depressor palsy (HP:0020042)

Term ID:

20042

Name:

Double depressor palsy

Synonym:

Definition:

An ocular movement abnormality characterised by simultaneous weakness of the inferior rectus muscle and superior oblique muscle of the same eye.

Comments:

Reference:

HP:0020042

Genes and Diseases:

Child Nodes:

Sister Nodes:

Brown anomaly (HP:0031622)

Double elevator palsy (HP:0020041)

Duane anomaly (HP:0009921)

Horizontal incomitant strabismus (HP:0020044)

Vertical incomitant strabismus (HP:0020043)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0020042	HP:0020042	Double depressor palsy	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.