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 eye physiology (HP:0012373)

Parent Node:
Abnormality of eye movement (HP:0000496)

..Starting node
..Impaired ocular adduction (HP:0000542)

Term ID:

542

Name:

Impaired ocular adduction

Synonym:

Definition:

Reduced ability to move the eye in the direction of the nose.

Comments:

Reference:

HP:0000542

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal conjugate eye movement (HP:0000549)

Abnormal involuntary eye movements (HP:0012547)

Abnormal ocular alignment (HP:0500073)

Abnormal saccadic eye movements (HP:0000570)

Abnormal visual fixation (HP:0025404)

Abnormality of ocular abduction (HP:0011347)

Abnormality of ocular smooth pursuit (HP:0000617)

Compensatory head posture (HP:0031705)

Limited extraocular movements (HP:0007941)

Marcus Gunn jaw winking synkinesis (HP:0025186)

Oculomotor apraxia (HP:0000657)

Ophthalmoparesis (HP:0000597)

Visual gaze preference (HP:0025518)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	DiseaseId	DiseaseName	DiseaseMIM	ConceptID	Source	Typical association	ClinVar variants	HGNC ID	GeneMIM
HPO disease - gene - phenotype typical associations:
HP:0000542	HP:0000542	Impaired ocular adduction	0	MAFB CL E G H	9935	617041	Duane retraction syndrome 3 with or without deafness	617041	C4310752	OMIM	1	153	6408	608968
HP:0000542	HP:0000542	Impaired ocular adduction	0	SALL4 CL E G H	57167	607323	Duane-radial ray syndrome	607323	C1623209	OMIM	1	301	15924	607343
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (2) :MAFB SALL4

Diseases (2) :617041 607323

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.