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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: Vision Disorders (D014786)
..Starting node ..Night Blindness (D009755)
Child Nodes:
........CSNB1C (C567704)
........Fleck Retina of Kandori (C562701)
........Night blindness skeletal anomalies unusual facies (C536121)
........Night blindness, congenital stationary (C536122) 4
........Night Blindness, Congenital Stationary, Autosomal Dominant 1 (C566474)
........Night Blindness, Congenital Stationary, Autosomal Dominant 2 (C566869)
........Night Blindness, Congenital Stationary, Autosomal Dominant 3 (C566475)
........NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (OMIM:610427)
........Oguchi disease (C537743)
........Retinopathy, Pericentral Pigmentary, Dominant (C566713)
Sister Nodes:
..Alice in Wonderland Syndrome (D062026)
..Amblyopia (D000550) 2
..Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction (C563394)
..Blindness (D001766) 39
..Color Vision Defects (D003117) 11
..Creutzfeldt-Jakob Disease, Heidenhain Variant (C566981)
..Diplopia (D004172)
..Enhanced S-Cone Syndrome (C564835)
..Hemianopsia (D006423)
..Night Blindness (D009755) 14
..Photophobia (D020795) 2
..Scotoma (D012607) 1
..Siegler Brewer Carey syndrome (C537335)
..SPATIAL VISUALIZATION, APTITUDE FOR (OMIM:313000)
..Susac Syndrome (D055955)
..Vision, Low (D015354)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8066
Name:	Night Blindness
Definition:	Failure or imperfection of vision at night or in dim light, with good vision only on bright days. (Dorland, 27th ed)
Alternative IDs:
ParentIDs:	MESH:D014786
TreeNumbers:	C11.966.671
Synonyms:	Blindness, Night \|Nyctalopia
Slim Mappings:	Eye disease
Reference:	MedGen: D009755 MeSH: D009755 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants