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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 ..Esotropia (D004948)
Child Nodes:
........Goldblatt Viljoen syndrome (C537280)
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:	4000
Name:	Esotropia
Definition:	A form of ocular misalignment characterized by an excessive convergence of the visual axes, resulting in a 'cross-eye' appearance. An example of this condition occurs when paralysis of the lateral rectus muscle causes an abnormal inward deviation of one eye on attempted gaze.
Alternative IDs:
ParentIDs:	MESH:D013285
TreeNumbers:	C10.292.562.887.300 \|C11.590.810.400
Synonyms:	Convergent Strabismus \|Cross Eye \|Cross-Eye \|Cross-Eyes \|Esodeviation \|Esodeviations \|Esophoria \|Esophorias \|Esotropia, Intermittent \|Esotropia, Monocular \|Esotropia, Primary \|Esotropias \|Esotropia, Secondary \|Esotropias, Intermittent \|Esotropias, Monocular \|Esotropias
Slim Mappings:	Eye disease\|Nervous system disease
Reference:	MedGen: D004948 MeSH: D004948 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants