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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

Disease Browser
Parent Node: Strabismus (D013285)
..Starting node ..Exotropia (D005099)
Child Nodes:
Sister Nodes:
..Carnevale syndrome (C535586)
..Esotropia (D004948) 1
..Exotropia (D005099)
..Hemifacial Hyperplasia With Strabismus (C564199)
..Krauss Herman Holmes syndrome (C537618)
..McPherson Robertson Cammarano syndrome (C538161)
..Mehes syndrome (C536146)
..MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS (OMIM:613671)
..Ptosis, Strabismus, And Ectopic Pupils (C566736)
..Singh Chhaparwal Dhanda syndrome (C537341)
..Speech Development, Delayed, With Facial Asymmetry, Strabismus, And Transverse Earlobe Crease (C566677)
..Van Bogaert-Hozay syndrome (C536526)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4031
Name:	Exotropia
Definition:	A form of ocular misalignment where the visual axes diverge inappropriately. For example, medial rectus muscle weakness may produce this condition as the affected eye will deviate laterally upon attempted forward gaze. An exotropia occurs due to the relatively unopposed force exerted on the eye by the lateral rectus muscle, which pulls the eye in an outward direction.
Alternative IDs:
ParentIDs:	MESH:D013285
TreeNumbers:	C10.292.562.887.650 \|C11.590.810.440
Synonyms:	Alternating Exotropia \|Divergent Strabismus \|Exodeviation \|Exodeviations \|Exophoria \|Exotropia, Alternating \|Exotropia, Monocular \|Exotropia, Primary \|Exotropia, Secondary \|Monocular Exotropia \|Primary Exotropia \|Secondary Exotropia \|Strabismus, Divergent
Slim Mappings:	Eye disease\|Nervous system disease
Reference:	MedGen: D005099 MeSH: D005099 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants