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QuickView for anhidrosis (phenotype)


Genetic Markers

Most Correlated Genes

Most Correlated SNPs

  1. ITPR2
  1. No SNPs found
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Pathway Enrichment

Most Correlated Biogroups

  1. Inositol 1,4,5-trisphosphate receptor
  2. RyR/IP3R Homology associated domain
  3. Ryanodine receptor-related
  4. RyR/IP3 receptor binding core, RIH domain superfamily
  5. RIH domain
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Curated Studies

Most Correlated Studies

  1. Mouse Phenotypes - Hereditary peripheral neuropathy
  2. OMIM - Neuropathy
  3. OMIM - Anhidrosis
  4. OMIM - Pain
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Literature

Most Relevant Literature

  1. Reduced Myocardial Uptake of 123I-MIBG in Congenital Insensitivity to Pain With Anhidrosis.
  2. Ion Channel and Ubiquitin Differential Expression during Erythromycin-Induced Anhidrosis in Foals.
  3. Case Study of a Rare Genetic Disorder: Congenital Insensitivity to Pain With Anhidrosis.
  4. Genomic Association of Chronic Idiopathic Anhidrosis to a Potassium Channel Subunit in a Large Anima…
  5. The 482nd case: vomiting, paroxysmal dizziness and anhidrosis].
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Clinical Trials

Most Relevant Clinical Trials

  1. A Study of Norepinephrine in Patients With Congenital Insensitivity to Pain and Anhidrosis
  2. The Effects of Horner's Syndrome Developing After Interscalene Brachial Plexus Block on Autonomic Ne…
  3. A Novel Noninvasive Thermoregulatory Device for Postural Tachycardia Syndrome
  4. Changes in Skin Conductance Measurement as an Endpoint Monitor for Sympathetic Blocks
  5. Electrical Skin Conductance Monitoring as an Assessment of Post Operative Pain Scores
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