Hyperhidrosis
Symptom Information:
Symptom ID: | HPO:0000975 | |||||||||||||||||||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||||||||||||||||||
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) |