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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: Sweat Gland Diseases (D013543)
..Starting node ..Hyperhidrosis (D006945)
Child Nodes:
........Book Syndrome (C562993)
........Cold-Induced Sweating Syndrome 1 (C564791)
........Granulosis Rubra Nasi (C562483)
........HYPERCHLORHIDROSIS, ISOLATED (OMIM:143860)
........Hyperhidrosis Palmaris Et Plantaris (C563185)
........Shapiro syndrome (C537594)
........Sweating, Gustatory (D013547)
Sister Nodes:
..Hidradenitis (D016575) 2
..Hyperhidrosis (D006945) 7
..Hypohidrosis (D007007) 9
..Miliaria (D008883) 2
..Sweat Gland Neoplasms (D013544)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5382
Name:	Hyperhidrosis
Definition:	Excessive sweating. In the localized type, the most frequent sites are the palms, soles, axillae, inguinal folds, and the perineal area. Its chief cause is thought to be emotional. Generalized hyperhidrosis may be induced by a hot, humid environment, by fever, or by vigorous exercise.
Alternative IDs:
ParentIDs:	MESH:D013543
TreeNumbers:	C17.800.946.350
Synonyms:
Slim Mappings:	Skin disease
Reference:	MedGen: D006945 MeSH: D006945 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants