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:
Abnormal horizontal rectus muscle physiology (HP:0031740)

Parent Node:
Abnormal lateral rectus muscle physiology (HP:0031749)

..Starting node
..Lateral rectus muscle weakness (HP:0031750)

Term ID:

31750

Name:

Lateral rectus muscle weakness

Synonym:

Definition:

Decreased strength (ability to move) of the lateral rectus muscle.

Comments:

Reference:

HP:0031750

Genes and Diseases:

Child Nodes:

........

Lateral rectus muscle underaction (HP:0031751)

........

Lateral rectus muscle restriction (HP:0031758)

Sister Nodes:

Lateral rectus muscle overaction (HP:0031752)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031750	HP:0031750	Lateral rectus muscle weakness	0	CL E G H
HP:0031750	HP:0031758	Lateral rectus muscle restriction	1	CL E G H
HP:0031750	HP:0031751	Lateral rectus muscle underaction	1	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.