COCH, cochlin, 1690

N. diseases: 45; N. variants: 14
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C1832425
Disease: Deafness, Autosomal Dominant 9
Deafness, Autosomal Dominant 9
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 4 10 0.990 strong 1.000 23 10 1998 2017
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 740 337 0.400 strong 0.909 11 2 1999 2019
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 163 66 0.340 definitive 1.000 14 1 1998 2017
Sensorineural hearing loss, bilateral
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 117 30 0.220 None 1.000 4 1 2008 2019
Sensorineural Hearing Loss (disorder)
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 783 111 0.200 None 0.923 13 2 2001 2019
CUI: C0042571
Disease: Vertigo
Vertigo
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Sign or Symptom 173 35 0.120 None 1.000 2 2003 2016
CUI: C0040264
Disease: Tinnitus
Tinnitus
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 103 14 0.110 None 1.000 1 2013 2013
Prelingual sensorineural hearing impairment
disease Disease or Syndrome 17 7 0.100 None 1.000 1 1 2018 2018
Platelet mean volume determination (procedure)
phenotype Laboratory Procedure 223 371 0.100 None 1.000 1 1 2016 2016
CUI: C1849095
Disease: Cochlear degeneration
Cochlear degeneration
phenotype Finding 3 0.100 None 0
CUI: C1843865
Disease: Vestibular dysfunction
Vestibular dysfunction
phenotype Finding 16 0.100 None 0
CUI: C3554568
Disease: Young adult onset
Young adult onset
phenotype Finding 8 0.100 None 0
Postlingual sensorineural hearing impairment
phenotype Pathologic Function 2 0.100 None 0
Abnormality of the vestibulocochlear nerve
disease Anatomical Abnormality 2 0.100 None 0
CUI: C0042594
Disease: Vestibular Diseases
Vestibular Diseases
group Otorhinolaryngologic Diseases Disease or Syndrome 10 0.060 None 1.000 6 2001 2016
CUI: C0494559
Disease: Diseases of inner ear
Diseases of inner ear
group Otorhinolaryngologic Diseases Disease or Syndrome 4 0.060 None 1.000 6 2001 2016
Progressive sensorineural hearing impairment
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 78 28 0.050 None 1.000 5 1 1996 2018
CUI: C0025281
Disease: Meniere Disease
Meniere Disease
disease Otorhinolaryngologic Diseases Disease or Syndrome 69 36 0.050 None 1.000 5 1999 2016
CUI: C0595921
Disease: Intraocular pressure disorder
Intraocular pressure disorder
disease Eye Diseases Disease or Syndrome 304 56 0.030 None 1.000 3 2012 2017
CUI: C0395971
Disease: Dominant sensorineural hearing loss
Dominant sensorineural hearing loss
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 6 1 0.020 None 1.000 2 2004 2016
Autoimmune sensorineural hearing loss
disease Pathological Conditions, Signs and Symptoms; Immune System Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 1 0.020 None 1.000 2 2005 2006
CUI: C1838701
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 2
DEAFNESS, AUTOSOMAL RECESSIVE 2
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 7 135 0.010 None 1.000 1 2002 2002
CUI: C1848641
Disease: Profound sensorineural hearing loss
Profound sensorineural hearing loss
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 22 4 0.010 None 1.000 1 1 2018 2018
Profound sensorineural hearing impairment
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 10 2 0.010 None 1.000 1 2018 2018
CUI: C1866095
Disease: Deafness, Autosomal Dominant 13
Deafness, Autosomal Dominant 13
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 6 3 0.010 None 1.000 1 2002 2002