Anhidrosis

Alias:
Hypohidrosis
Absence of Sweating
Impaired Sweating
Oligohidrosis
Adiaphoresis
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Anhidrosis, also known as hypohidrosis, is related to insensitivity to pain, congenital, with anhidrosis and neuropathy, hereditary sensory and autonomic, type v, and has symptoms including hyperthermia and increased sweating. An important gene associated with Anhidrosis is ITPR2 (Inositol 1,4,5-Trisphosphate Receptor Type 2), and among its related pathways/superpathways are Innate Immune System and GPCR Pathway. Affiliated tissues include skin and spinal cord, and related phenotypes are Decreased viability and Increased human cytomegalovirus (HCMV) strain AD169 replication
Related ID:
MESH:D007007
ICD11:1299624490

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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21
218
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Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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