ADAM9, ADAM metallopeptidase domain 9, 8754

N. diseases: 109; N. variants: 6
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: C1423873
Disease: CONE-ROD DYSTROPHY 9
CONE-ROD DYSTROPHY 9 		disease Disease or Syndrome 1 5 0.810 None 1.000 6 5 2002 2014
CUI: C1858806
Disease: CONE-ROD DYSTROPHY 3 (disorder)
CONE-ROD DYSTROPHY 3 (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 3 53 0.010 None 1.000 1 2010 2010
CUI: C4551465
Disease: Small airways disease
Small airways disease 		disease Disease or Syndrome 4 0.010 None 1.000 1 2018 2018
CUI: C0521691
Disease: Generalized progressive retinal atrophy
Generalized progressive retinal atrophy 		disease Disease or Syndrome 5 0.010 None 1.000 1 2010 2010
CUI: C0278493
Disease: Breast cancer recurrent
Breast cancer recurrent 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 41 0.010 None 1.000 1 2005 2005
CUI: C0010246
Disease: Coxsackievirus Infections
Coxsackievirus Infections 		group Infections Disease or Syndrome 48 1 0.010 None < 0.001 1 2019 2019
CUI: C0206702
Disease: Klatskin Tumor
Klatskin Tumor 		disease Neoplasms Neoplastic Process 50 0.010 None 1.000 1 2018 2018
CUI: C0858617
Disease: Posterior subcapsular cataract
Posterior subcapsular cataract 		disease Eye Diseases Disease or Syndrome 67 9 0.010 None 1.000 1 2014 2014
CUI: C0751075
Disease: Cancer of Digestive System
Cancer of Digestive System 		disease Digestive System Diseases; Neoplasms Neoplastic Process 71 15 0.010 None 1.000 1 2019 2019
CUI: C1402294
Disease: Primary Lesion
Primary Lesion 		phenotype Disease or Syndrome 71 8 0.010 None 1.000 1 2010 2010
CUI: C1333977
Disease: Hepatitis B Virus-Related Hepatocellular Carcinoma
Hepatitis B Virus-Related Hepatocellular Carcinoma 		disease Neoplastic Process 76 8 0.010 None 1.000 1 2017 2017
CUI: C0036205
Disease: Sarcoidosis, Pulmonary
Sarcoidosis, Pulmonary 		disease Respiratory Tract Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 81 1 0.010 None 1.000 1 2013 2013
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 86 53 0.130 None 1.000 3 2 2009 2014
CUI: C0009398
Disease: Color vision defect
Color vision defect 		phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 94 4 0.100 None 0
CUI: C0014868
Disease: Esophagitis
Esophagitis 		disease Digestive System Diseases Disease or Syndrome 105 7 0.010 None 1.000 1 2017 2017
CUI: C1333001
Disease: Childhood Renal Cell Carcinoma
Childhood Renal Cell Carcinoma 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 107 10 0.010 None 1.000 1 2008 2008
CUI: C0276138
Disease: Viral myocarditis
Viral myocarditis 		disease Infections; Cardiovascular Diseases Disease or Syndrome 129 2 0.010 None 1.000 1 2019 2019
CUI: C0206650
Disease: Fibroadenoma
Fibroadenoma 		disease Neoplasms Neoplastic Process 151 1 0.010 None 1.000 1 2003 2003
CUI: C0521707
Disease: Bilateral cataracts (disorder)
Bilateral cataracts (disorder) 		disease Eye Diseases Disease or Syndrome 166 37 0.010 None 1.000 1 2002 2002
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		disease Eye Diseases Disease or Syndrome 168 18 0.100 None 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 194 33 0.030 None 1.000 3 2009 2014
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		phenotype Finding 215 5 0.100 None 0
CUI: C0085636
Disease: Photophobia
Photophobia 		phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Sign or Symptom 227 7 0.100 None 0
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 254 51 0.330 None 1.000 3 2009 2014
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 267 80 0.010 None 1.000 1 2005 2005