Hyperhidrosis

Symptom Information:

Symptom ID: HPO:0000975
Synonyms:
Diaphoresis [HPO:0000975]
Increased sweating [HPO:0000975]
Sweating [HPO:0000975]
Hyperhidrosis (disorder) [Orphanet:23010]
Excessive sweating (finding) [Orphanet:23010]
Hyperhidrosis disorder [Orphanet:23010]
Increased sweating [Orphanet:23010]
Diaphoresis [OMIM:Diaphoresis]
Hyperhidrosis [OMIM:Hyperhidrosis]
Increased sweating [OMIM:Increased sweating]
Sweating [OMIM:Sweating]
Hyperhidrosis/increased sweating [Orphanet:23010]
Hyperhidrosis [Orphanet:23010]
Perspiration excessive [Orphanet:23010]
Sweating increased [Orphanet:23010]
Hyperhidrosis [MedDRA:10020642]
Diaphoresis [MedDRA:10020642]
Drenching sweats [MedDRA:10020642]
Excess sweating [MedDRA:10020642]
Heavy sweating [MedDRA:10020642]
Hot &
sweaty [MedDRA:10020642]
Perspiration excessive [MedDRA:10020642]
Sweating [MedDRA:10020642]
Sweating attack [MedDRA:10020642]
Sweating easily [MedDRA:10020642]
Sweating increased [MedDRA:10020642]
Sweating increased armpits [MedDRA:10020642]
Sweating increased palms [MedDRA:10020642]
Sweaty [MedDRA:10020642]
Sweaty plams [MedDRA:10020642]
Sweaty hands [MedDRA:10020642]
Plantar hyperhidrosis [MedDRA:10020642]
Sudation increased [MedDRA:10020642]
Sudoresis [MedDRA:10020642]
Excessive sweating (autonomic involvement) [OMIM:Excessive sweating (autonomic involvement)]
Hyperhidrosis (hands and feet) [OMIM:Hyperhidrosis (hands and feet)]
Hyperhidrosis (in some patients) [OMIM:Hyperhidrosis (in some patients)]
Hyperhidrosis (palms and soles) [OMIM:Hyperhidrosis (palms and soles)]
Quality:
Cross references:
HPO:0001064 "Diaphoresis" [Orphanet:23010]
Orphanet:23010 "Hyperhidrosis/increased sweating" [Orphanet:23010]
OMIM: "Diaphoresis" [OMIM:Diaphoresis]
OMIM: "Hyperhidrosis" [OMIM:Hyperhidrosis]
OMIM: "Increased sweating" [OMIM:Increased sweating]
OMIM: "Sweating" [OMIM:Sweating]
OMIM: "Excessive sweating (autonomic involvement)" [OMIM:Excessive sweating (autonomic involvement)]
OMIM: "Hyperhidrosis (hands and feet)" [OMIM:Hyperhidrosis (hands and feet)]
OMIM: "Hyperhidrosis (in some patients)" [OMIM:Hyperhidrosis (in some patients)]
OMIM: "Hyperhidrosis (palms and soles)" [OMIM:Hyperhidrosis (palms and soles)]
UMLS:C0020458 "Hyperhidrosis" [HPO:0000975]
UMLS:C0700590 "Diaphoresis" [HPO:0000975]
UMLS:C0020458 "Hyperhidrosis disorder" [Orphanet:23010]
UMLS:C0700590 "Increased sweating" [Orphanet:23010]
Is a (Direct Parents):
HPO         Night sweats
MedDRA General signs and symptoms NEC
Orphanet Abnormality of the skin
HPO         Abnormality of the sweat gland
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of skin adnexa(HPO:0011138)
             Abnormality of the sweat gland(HPO:0000971)
                Hyperhidrosis(HPO:0000975)
MedDRA:
General disorders and administration site conditions(MedDRA:10018065)
    General system disorders NEC(MedDRA:10018073)
       General signs and symptoms NEC(MedDRA:10018072)
          Hyperhidrosis(HPO:0000975)
Database Frequency: 64 / 7739
Resource:

All diseases associated with this symptom:

ANGIOKERATOMA CORPORIS DIFFUSUM WITH ARTERIOVENOUS FISTULAS (OMIM:600419)
Aromatic L-amino acid decarboxylase deficiency (Orphanet:35708)
Autosomal recessive axonal neuropathy with neuromyotonia (Orphanet:324442)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Bloom syndrome (Orphanet:125)
Buerger disease (Orphanet:36258)
Böök syndrome (Orphanet:1262)
CARDIOFACIOCUTANEOUS SYNDROME 3 (OMIM:615279)
CARDIOFACIOCUTANEOUS SYNDROME 4 (OMIM:615280)
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM (OMIM:118301)
CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE (OMIM:118230)
CLUSTER HEADACHE, FAMILIAL (OMIM:119915)
COLD-INDUCED SWEATING SYNDROME 2 (OMIM:610313)
Cold-induced sweating syndrome (Orphanet:157820)
Congenital muscular dystrophy, Ullrich type (Orphanet:75840)
Cranio-osteoarthropathy (Orphanet:1525)
Diffuse palmoplantar keratoderma with painful fissures (Orphanet:369999)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
Ectodermal dysplasia - cutaneous syndactyly syndrome (Orphanet:247827)
Fatal familial insomnia (Orphanet:466)
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency (Orphanet:289527)
Fatal infantile lactic acidosis with methylmalonic aciduria (Orphanet:17)
Focal palmoplantar keratoderma with joint keratoses (Orphanet:370002)
Fucosidosis (Orphanet:349)
GRANULOSIS RUBRA NASI (OMIM:139000)
GRAVES DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:275000)
Glycogen storage disease due to glucose-6-phosphatase deficiency type a (Orphanet:79258)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
HYPERHIDROSIS, GUSTATORY (OMIM:144100)
HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL DOMINANT (OMIM:167100)
Haddad syndrome (Orphanet:99803)
Hereditary pheochromocytoma-paraganglioma (Orphanet:29072)
Hereditary sensory and autonomic neuropathy type 6 (Orphanet:314381)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hyperinsulinism-hyperammonemia syndrome (Orphanet:35878)
Leigh syndrome (Orphanet:506)
Leprechaunism (Orphanet:508)
Mal de Meleda (Orphanet:87503)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII (OMIM:615548)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Ondine syndrome (Orphanet:661)
PACHYONYCHIA CONGENITA 3 (OMIM:615726)
PARAGANGLIOMAS 1 (OMIM:168000)
PARAGANGLIOMAS 1 (OMIM:168000)
PARAGANGLIOMAS 3 (OMIM:605373)
PARAGANGLIOMAS 3 (OMIM:605373)
PARAGANGLIOMAS 4 (OMIM:115310)
PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME (OMIM:171420)
PHEOCHROMOCYTOMAPHEOCHROMOCYTOMA, SUSCEPTIBILITY TO (OMIM:171300)
Pachydermoperiostosis (Orphanet:2796)
Peripheral motor neuropathy - dysautonomia (Orphanet:2400)
Primary erythermalgia (Orphanet:90026)
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 (OMIM:604320)
Sandhoff disease, infantile form (Orphanet:309155)
Sodium channelopathy-related small fiber neuropathy (Orphanet:306577)
Spastic paraplegia-optic atrophy-neuropathy syndrome (Orphanet:320406)
Spinal muscular atrophy with respiratory distress (Orphanet:98920)
Stiff person syndrome (Orphanet:3198)
Tyrosinemia type 2 (Orphanet:28378)
Wolfram syndrome 1 (OMIM:222300)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)