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QuickView for hearing loss (phenotype)


Genetic Markers

Most Correlated Genes

Most Correlated SNPs

  1. SPTBN4
  2. BCS1L
  3. HPPD
  4. CIHL
  5. GAS2
  1. No SNPs found
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Pathway Enrichment

Most Correlated Biogroups

  1. sensory perception of mechanical stimulus
  2. inner ear development
  3. embryonic organ morphogenesis
  4. ATPase, AAA-type, conserved site
  5. ATPase, AAA-type, core
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Curated Studies

Most Correlated Studies

  1. Mouse Phenotypes - Degenerative disease of the CNS
  2. Mouse Phenotypes - Disorder of head
  3. OMIM - Hearing impairment
  4. OMIM - Hearing loss associated with syndrome
  5. Lymphoblastoid lines of family with maternally inherited non-syndromic hearing loss
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Literature

Most Relevant Literature

  1. Novel genetic syndrome manifesting with cerebral atrophy, cataract, hypoacusis, diabetes, and brachy…
  2. Rare Gene Mutations in Romanian Hypoacusis Patients: Case Series and a Review of the Literature.
  3. Sudden hearing loss after dental treatment.
  4. c-Ret-mediated hearing losses.
  5. Homozygosity mapping identifies a novel GIPC3 mutation causing congenital nonsyndromic hearing loss …
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Clinical Trials

Most Relevant Clinical Trials

  1. Hearing Loss Prevention for Veterans
  2. Fatigue and Hearing Loss.
  3. Cognitive Screening Of Patients With Hearing Loss
  4. Hearing Loss and Osteoporosis
  5. FX-322 in Sensorineural Hearing Loss
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