MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

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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

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: vision disorder (MONDO:0021084)
..Starting node ..binocular vision disease ()
Child Nodes:
........abnormal retinal correspondence ()
Sister Nodes:
..Alice in wonderland syndrome ()
..amblyopia (disease) ()
..binocular vision disease ()
..blindness (disorder) ()
..cerebral visual impairment ()
..visual agnosia (disease) ()
..visual pathway disease ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1564
Name:	binocular vision disease
Definition:	Any inability to efficiently utilize and/or sustain binocular vision.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	binocular vision disorder; simultaneous visual perception without fusion
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal