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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: Primary Dysautonomias (D054969)
..Starting node ..Dysautonomia like disorder (C535728)
Child Nodes:
Sister Nodes:
..Acute cholinergic dysautonomia (C535672)
..Dysautonomia like disorder (C535728)
..Dysautonomia, Familial (D004402) 1
..Multiple System Atrophy (D019578) 21
..Orthostatic Intolerance (D054971) 8
..Pure Autonomic Failure (D054970)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3502
Name:	Dysautonomia like disorder
Definition:
Alternative IDs:
ParentIDs:	MESH:D054969
TreeNumbers:	C10.177.575/C535728
Synonyms:	Dysautonomia-Like Disorder
Slim Mappings:	Nervous system disease
Reference:	MedGen: C535728 MeSH: C535728 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants