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: C0152459
Disease: Linear atrophy
Linear atrophy
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 149 6 0.010 None 1.000 1 2007 2007
Morphological abnormality of the vestibule of the inner ear
group Anatomical Abnormality 2 0.010 None 1.000 1 2000 2000
Abnormality of the vestibulocochlear nerve
disease Anatomical Abnormality 2 0.100 None 0
CUI: C3698167
Disease: Congenital prelingual deafness
Congenital prelingual deafness
disease Congenital Abnormality 1 1 0.010 None 1.000 1 1 2018 2018
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: 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 (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: 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: 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
CUI: C0025281
Disease: Meniere Disease
Meniere Disease
disease Otorhinolaryngologic Diseases Disease or Syndrome 69 36 0.050 None 1.000 5 1999 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
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
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: C0017601
Disease: Glaucoma
Glaucoma
disease Eye Diseases Disease or Syndrome 770 198 0.010 None 1.000 1 2007 2007
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
disease Eye Diseases Disease or Syndrome 168 18 0.010 None < 0.001 1 2010 2010
CUI: C0028841
Disease: Ocular Hypotension
Ocular Hypotension
disease Eye Diseases Disease or Syndrome 22 1 0.010 None 1.000 1 2012 2012
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
CUI: C0042974
Disease: von Willebrand Disease
von Willebrand Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 62 78 0.010 None 1.000 1 2008 2008
CUI: C0079474
Disease: Hallopeau-Siemens Disease
Hallopeau-Siemens Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 51 54 0.010 None 1.000 1 2018 2018
CUI: C0271514
Disease: Low frequency deafness
Low frequency deafness
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 15 1 0.010 None 1.000 1 2002 2002
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle
disease Eye Diseases Disease or Syndrome 383 222 0.010 None < 0.001 1 2013 2013
CUI: C0524851
Disease: Neurodegenerative Disorders
Neurodegenerative Disorders
group Nervous System Diseases Disease or Syndrome 1515 85 0.010 None 1.000 1 2006 2006