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:
Abnormal extraocular muscle physiology (HP:0025590)

Parent Node:
Abnormal rectus muscle physiology (HP:0031755)

..Starting node
..Abnormal horizontal rectus muscle physiology (HP:0031740)

Term ID:

31740

Name:

Abnormal horizontal rectus muscle physiology

Synonym:

Definition:

A functional anomaly of the medial rectus muscle or lateral rectus muscle.

Comments:

Reference:

HP:0031740

Genes and Diseases:

Child Nodes:

........

Abnormal medial rectus muscle physiology (HP:0025606)

................... HP:0031753 Medial rectus muscle weakness
................... HP:0031754 Medial rectus muscle overaction

........

Abnormal lateral rectus muscle physiology (HP:0031749)

................... HP:0031750 Lateral rectus muscle weakness
................... HP:0031752 Lateral rectus muscle overaction

Sister Nodes:

Abnormal vertical rectus muscle physiology (HP:0031748)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031740	HP:0031740	Abnormal horizontal rectus muscle physiology	0	CL E G H
HP:0031740	HP:0031749	Abnormal lateral rectus muscle physiology	1	CL E G H
HP:0031740	HP:0025606	Abnormal medial rectus muscle physiology	1	CL E G H
HP:0031740	HP:0031754	Medial rectus muscle overaction	2	CL E G H
HP:0031740	HP:0031753	Medial rectus muscle weakness	2	CL E G H
HP:0031740	HP:0031752	Lateral rectus muscle overaction	2	CL E G H
HP:0031740	HP:0031750	Lateral rectus muscle weakness	2	CL E G H
HP:0031740	HP:0031756	Medial rectus muscle underaction	3	CL E G H
HP:0031740	HP:0031751	Lateral rectus muscle underaction	3	CL E G H
HP:0031740	HP:0031758	Lateral rectus muscle restriction	3	CL E G H
HP:0031740	HP:0031757	Medial rectus muscle restriction	3	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.