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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: Nystagmus, Pathologic (D009759)
..Starting node ..Hereditary vertical nystagmus (C537857)
Child Nodes:
Sister Nodes:
..Episodic ataxia with nystagmus (C535506)
..Hereditary vertical nystagmus (C537857)
..Neuhauser Daly Magnelli syndrome (C536406)
..Nystagmus, Congenital (D020417) 17
..Nystagmus, Myoclonic (C564088)
..Singh Chhaparwal Dhanda syndrome (C537341)
..Split hand split foot nystagmus (C537319)
..Zonular cataract and nystagmus (C536727)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5124
Name:	Hereditary vertical nystagmus
Definition:
Alternative IDs:
ParentIDs:	MESH:D009759
TreeNumbers:	C10.292.562.675/C537857 \|C11.590.400/C537857
Synonyms:	Congenital hereditary vertical nystagmus \|Nystagmus, hereditary vertical
Slim Mappings:	Eye disease\|Nervous system disease
Reference:	MedGen: C537857 MeSH: C537857 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants