Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Brain Diseases (D001927)
Parent Node: Hashimoto Disease (D050031)
..Starting node ..Hashimoto's encephalitis (C535841)
Child Nodes:
Sister Nodes:
..Hashimoto's encephalitis (C535841)
..Hypothyroidism, Autoimmune (C562768)
..Thyroiditis, Chronic (C535842)
..THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1 (OMIM:188580)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4907
Name:	Hashimoto's encephalitis
Definition:
Alternative IDs:
ParentIDs:	MESH:D001927\|MESH:D050031
TreeNumbers:	C10.228.140/C535841 \|C19.874.871.102.500/C535841
Synonyms:	Autoimmune encephalitis \|Hashimoto's encephalopathy \|Steroid-responsive encephalopathy associated with autoimmune thyroiditis
Slim Mappings:	Endocrine system disease\|Nervous system disease
Reference:	MedGen: C535841 MeSH: C535841 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants