Aliases & Classifications for Hypohidrosis

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Aliases & Descriptions for Hypohidrosis:

Name: Hypohidrosis 10 47 12 36 65
 
Oligohidrosis 10

Classifications:



External Ids:

Disease Ontology10 DOID:11155
ICD1027 L74.4
SNOMED-CT59 201189007, 45004005
MeSH36 D007007
NCIt42 C34718
UMLS65 C0020620

Summaries for Hypohidrosis

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Wikipedia:68 Hypohidrosis is diminished sweating in response to appropriate stimuli. While hyperhidrosis is a... more...

MalaCards based summary: Hypohidrosis, also known as oligohidrosis, is related to ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant and ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant. An important gene associated with Hypohidrosis is COG6 (Component Of Oligomeric Golgi Complex 6), and among its related pathways is . Affiliated tissues include skin, breast and brain, and related mouse phenotypes are pigmentation and respiratory system.

Related Diseases for Hypohidrosis

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Diseases related to Hypohidrosis via text searches within MalaCards or GeneCards Suite gene sharing:

(show top 50)    (show all 84)
idRelated DiseaseScoreTop Affiliating Genes
1ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant30.7EDAR, EDARADD
2ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant30.7EDAR, EDARADD
3hypohidrotic ectodermal dysplasia with hypothyroidism and ciliary dyskinesia30.5EDAR, EDARADD
4ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive30.5EDAR, EDARADD
5ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive30.0EDA, EDAR, EDARADD
6anhidrosis27.8ACHE, COG6, EDA, EDAR, EDARADD, GLA
7hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome12.3
8ectodermal dysplasia 3, witkop type11.5
9ichthyosis, congenital, autosomal recessive 1111.4
10hartnup disorder11.3
11ameloonychohypohidrotic syndrome11.3
12ichthyosis-hypotrichosis syndrome11.3
13shaheen syndrome10.4
14fabry disease10.4
15naegeli-franceschetti-jadassohn syndrome10.4
16lung cancer10.2
17hepatitis10.2
18leukemia10.2
19lymphoma10.2
20multiple endocrine neoplasia10.2
21headache10.2
22hypoxia10.2
23rapp-hodgkin syndrome10.2
24dermatopathia pigmentosa reticularis10.2
25ectodermal dysplasia 1, hypohidrotic, x-linked10.2
26hay-wells syndrome10.2
27ectodermal dysplasia10.2
28congenital ichthyosiform erythroderma10.2
29lelis syndrome10.2
30icos-related common variable immune deficiency10.2EDAR, EDARADD
31schizophrenia10.1
32pheochromocytoma10.1
33myocardial infarction10.1
34cystic fibrosis10.1
35endometrial cancer10.1
36marfan syndrome10.1
37nasopharyngeal carcinoma10.1
38acute myocardial infarction10.1
39alcohol abuse10.1
40b-cell lymphomas10.1
41bipolar disorder10.1
42diffuse large b-cell lymphoma10.1
43dilated cardiomyopathy10.1
44atrioventricular block10.1
45first-degree atrioventricular block10.1
46migraine with aura10.1
47natural killer cell leukemia10.1
48nasopharyngitis10.1
49gastroschisis10.1
50vertebrobasilar insufficiency10.1

Graphical network of the top 20 diseases related to Hypohidrosis:



Diseases related to hypohidrosis

Symptoms for Hypohidrosis

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Drugs & Therapeutics for Hypohidrosis

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Drugs for Hypohidrosis (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):

idNameStatusPhaseClinical TrialsCas NumberPubChem Id
1
Nitroprussideapproved5815078-28-111963622
Synonyms:
13755-38-9 (di-hydrochloride salt, diH20)
14402-89-2 (di-hydrochloride salt)
15078-28-1
C07269
CHEMBL74115
CID11953891
Disodium nitroprusside dihydrate
LS-187044
Nipride
Nitroferricyanide
 
Nitropress
Nitroprusside
Pentacyanidonitrosylferrate(2-)
Sodium Nitroprusside
Sodium nitroferricyanide dihydrate
Sodium nitroprusside
Sodium nitroprusside dihydrate
Sodium nitroprusside extra pure
UNII-169D1260KM
[Fe(CN)5(NO)](2-)
nitroferricyanide
2
Acetylcholineexperimental68951-84-3187
Synonyms:
ACh
Acetyl choline ion
Acetylcholine Chloride
Acetylcholine cation
 
Acetylcholinium: acetyl-Choline
Choline acetate
Choline acetate (ester)
Miochol E
O-Acetylcholine
acetylcholine chloride

Interventional clinical trials:

idNameStatusNCT IDPhase
1An Open-Label Clinical Trial of Replagal Enzyme Therapy in Children Ages 7-17 Years With Fabry DiseaseCompletedNCT00071877Phase 2
2Dosing Study of Replagal in Patients With Fabry DiseaseCompletedNCT00068107Phase 2
3Improving Autonomic Function and Balance in Diabetic NeuropathyRecruitingNCT01864460Phase 2
4Gene Therapy for Gaucher's and Fabry Disease Using Viruses and Blood-Forming CellsCompletedNCT00001234Phase 1
5Vasodilation in Patients With Fabry's DiseaseCompletedNCT00001774
6Analysis of the Nervous System in Patients With Fabry's DiseaseCompletedNCT00001491
7Pilot Study of the Effect of Laser on Reversing Chronic Radiation InjuryRecruitingNCT01910818
8Enzyme Replacement Therapy in Fabry DiseaseTerminatedNCT00149318

Search NIH Clinical Center for Hypohidrosis


Cochrane evidence based reviews: hypohidrosis

Genetic Tests for Hypohidrosis

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Anatomical Context for Hypohidrosis

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MalaCards organs/tissues related to Hypohidrosis:

33
Skin, Breast, Brain, Heart, Skeletal muscle, Lung, Myeloid

Animal Models for Hypohidrosis or affiliated genes

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MGI Mouse Phenotypes related to Hypohidrosis:

38
idDescriptionMGI Source AccessionScoreTop Affiliating Genes
1MP:00011869.3EDAR, EDARADD, KRT14
2MP:00053888.3ACHE, EDARADD, KRT14, TP63
3MP:00053827.3ACHE, EDAR, EDARADD, KRT14, TP63
4MP:00053917.2ACHE, EDAR, EDARADD, GLA, KRT14, TP63
5MP:00053787.1ACHE, EDAR, EDARADD, GLA, KRT14, TP63

Publications for Hypohidrosis

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Articles related to Hypohidrosis:

(show top 50)    (show all 72)
idTitleAuthorsYear
1
Gliomatosis cerebri in children shares molecular characteristics with other pediatric gliomas. (26744350)
2016
2
Successful treatment of tuberous sclerosis with psychosis and obsessive compulsive disorder: a case report. (25907259)
2015
3
Downregulation of miR-221, -30d, and -15a contributes to pathogenesis of prostate cancer by targeting Bmi-1. (25761682)
2015
4
Low expression levels of microRNA-124-5p correlated with poor prognosis in colorectal cancer via targeting of SMC4. (25081869)
2014
5
Association of the type of 5q loss with complex karyotype, clonal evolution, TP53 mutation status, and prognosis in acute myeloid leukemia and myelodysplastic syndrome. (24493299)
2014
6
Characteristic findings of handprint and dermoscopy in reticulate acropigmentation of Kitamura. (23746125)
2014
7
Misdiagnosing recurrent medulloblastoma: the danger of examination and imaging without histological confirmation. (24206345)
2014
8
Orchidectomy after primary chemotherapy for metastatic testicular cancer. (24021555)
2013
9
FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis. (23720823)
2013
10
Cyclosporine C2 Monitoring for the Treatment of Frequently Relapsing Nephrotic Syndrome in Children: A Multicenter Randomized Phase II Trial. (24262503)
2013
11
Protein carbamylation in chronic systolic heart failure: relationship with renal impairment and adverse long-term outcomes. (23582087)
2013
12
The macrophage migration inhibitory factor -173G/C polymorphism is not significantly associated with necrotizing enterocolitis in preterm infants. (23895962)
2013
13
A novel ARC gene polymorphism is associated with reduced risk of Alzheimer's disease. (22622366)
2012
14
Electrophysiological study with prophylactic pacing and survival in adults with myotonic dystrophy and conduction system disease. (22453570)
2012
15
Exploring the potential of flunarizine for Cisplatin-induced painful uremic neuropathy in rats. (22087421)
2011
16
Direct anti-cancer effect of oncostatin M on chondrosarcoma. (21344373)
2011
17
Quantitation of 17-OH-progesterone (OHPG) for diagnosis of congenital adrenal hyperplasia (CAH). (20077078)
2010
18
The neuropeptide VGF is reduced in human bipolar postmortem brain and contributes to some of the behavioral and molecular effects of lithium. (20631166)
2010
19
Increased expression of activation-induced cytidine deaminase is associated with anti-CCP and rheumatoid factor in rheumatoid arthritis. (19703021)
2009
20
Fulvestrant in advanced male breast cancer. (19752001)
2009
21
Triosephosphate isomerase and peroxiredoxin 6, two novel serum markers for human lung squamous cell carcinoma. (19737146)
2009
22
Basic fibroblast growth factor slow release stent graft for endovascular aortic aneurysm repair: a canine model experiment. (18639416)
2008
23
Reversing the effects of fragile X syndrome. (18645420)
2008
24
Case of metagonimiasis complicated with multiple intracerebral hemorrhages and diabetes mellitus. (18360077)
2008
25
Circulating oxidised low-density lipoprotein and intercellular adhesion molecule-1 and risk of type 2 diabetes mellitus: the Atherosclerosis Risk in Communities Study. (17136392)
2007
26
Differential modulation of gonadotropin secretion by selective estrogen receptor 1 and estrogen receptor 2 agonists in ovariectomized ewes. (17429013)
2007
27
Effects of N-methyl pyrrolidone on the uptake of hypericin in human bladder carcinoma and co-staining with DAPI investigated by confocal microscopy. (17877426)
2007
28
African tick bite fever. (17067925)
2006
29
Peripartum cardiomyopathy. (16371764)
2006
30
Expression of uncoupling protein 3 and GLUT4 gene in skeletal muscle of preterm newborns: possible control by AMP-activated protein kinase. (16966355)
2006
31
Inter-conversion of 7alpha- and 7beta-hydroxy-dehydroepiandrosterone by the human 11beta-hydroxysteroid dehydrogenase type 1. (16603347)
2006
32
Intravitreal triamcinolone acetonide treatment for serpiginous choroiditis. (17162609)
2006
33
Glomerular permeability activity: prevalence and prognostic value in pediatric patients with idiopathic nephrotic syndrome. (15384010)
2004
34
Tubulin polymerizing activity of dictyostatin-1, a polyketide of marine sponge origin. (12818367)
2003
35
Clonazepam in the long-term treatment of patients with unipolar depression, bipolar and schizoaffective disorder. (12650958)
2003
36
Does clinical diagnosis indicate ocular chlamydial infection in areas with a low prevalence of trachoma? (12187424)
2002
37
Pathogenesis and treatment of hypertension in polycystic kidney disease. (12187316)
2002
38
Therapeutic doses of oral methylphenidate significantly increase extracellular dopamine in the human brain. (11160455)
2001
39
Intra- and intermolecular beta-pleated sheet formation in glutamine-repeat inserted myoglobin as a model for polyglutamine diseases. (11584007)
2001
40
Detection of tongue cancer in primary care. (11217621)
2001
41
Atypical calcific tendinitis with cortical erosions. (11271549)
2000
42
Methylation of the BRCA1 promoter region in sporadic breast and ovarian cancer: correlation with disease characteristics. (10208417)
1999
43
Association of Ureaplasma urealyticum biovars with clinical outcome for neonates, obstetric patients, and gynecological patients with pelvic inflammatory disease. (9114407)
1997
44
The impact of hepatitis C antibody screening of source plasma donors on hepatitis C virus RNA in factor VIII concentrates. (27214632)
1995
45
Cysteine-string proteins as templates for membrane fusion: models of synaptic vesicle exocytosis. (7715197)
1995
46
cDNA cloning and sequence analysis of the bovine adrenocorticotropic hormone (ACTH) receptor. (8305507)
1994
47
Pediatric management problems. Neonatal abstinence syndrome. (2587106)
1989
48
Multiple-flap anoplasty in the treatment of rectal prolapse after pull-through operations for imperforate anus. (3819997)
1987
49
A review of the ultrasonic appearances of posterior urethral valve and ureteroceles. (3529016)
1986
50
The familial occurrence of hypoplastic right lung with systemic arterial supply and venous drainage "scimitar syndrome". (14426379)
1960

Variations for Hypohidrosis

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Expression for genes affiliated with Hypohidrosis

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Search GEO for disease gene expression data for Hypohidrosis.

Pathways for genes affiliated with Hypohidrosis

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Pathways related to Hypohidrosis according to GeneCards Suite gene sharing:

idSuper pathwaysScoreTop Affiliating Genes
1
Show member pathways
9.2

GO Terms for genes affiliated with Hypohidrosis

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Cellular components related to Hypohidrosis according to GeneCards Suite gene sharing:

idNameGO IDScoreTop Affiliating Genes
1apical part of cellGO:00451779.6EDA, EDAR

Biological processes related to Hypohidrosis according to GeneCards Suite gene sharing:

idNameGO IDScoreTop Affiliating Genes
1positive regulation of NF-kappaB import into nucleusGO:004234610.1EDA, EDAR
2pigmentationGO:00434739.8EDA, EDAR
3positive regulation of I-kappaB kinase/NF-kappaB signalingGO:00431239.6EDA, EDAR
4epithelial cell differentiationGO:00308559.4KRT14, TP63
5odontogenesis of dentin-containing toothGO:00424758.9EDA, EDAR, TP63
6cell differentiationGO:00301548.7EDA, EDAR, EDARADD, TP63

Sources for Hypohidrosis

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2CDC
14ExPASy
15FDA
16FMA
24GTR
25HGMD
26HMDB
27ICD10
28ICD10 via Orphanet
29ICD9CM
30IUPHAR
31KEGG
34MedGen
36MeSH
37MESH via Orphanet
38MGI
41NCI
42NCIt
43NDF-RT
46NINDS
47Novoseek
49OMIM
50OMIM via Orphanet
54PubMed
55QIAGEN
60SNOMED-CT via Orphanet
64Tumor Gene Family of Databases
65UMLS
66UMLS via Orphanet