ADAM10, ADAM metallopeptidase domain 10, 102

N. diseases: 202; N. variants: 8
Source: BEFREE ×
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: C0264270
Disease: Hypertrophic rhinitis
Hypertrophic rhinitis 		disease Infections; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 1 0.010 None 1.000 1 2016 2016
CUI: C0406811
Disease: Reticulate acropigmentation of Kitamura
Reticulate acropigmentation of Kitamura 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 2 0.720 strong 1.000 2 2013 2019
CUI: C0264732
Disease: Cardiac dilatation
Cardiac dilatation 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2006 2006
CUI: C0036457
Disease: Scrapie
Scrapie 		disease Infections; Nervous System Diseases; Animal Diseases Disease or Syndrome 6 0.010 None 1.000 1 2009 2009
CUI: C0948588
Disease: Lymphangiosis carcinomatosa
Lymphangiosis carcinomatosa 		disease Hemic and Lymphatic Diseases Neoplastic Process 8 0.010 None 1.000 1 2009 2009
CUI: C0085650
Disease: Purpura Fulminans
Purpura Fulminans 		disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 15 1 0.010 None 1.000 1 2018 2018
CUI: C0796149
Disease: Scott Syndrome
Scott Syndrome 		disease Hemic and Lymphatic Diseases Disease or Syndrome 15 0.010 None < 0.001 1 2019 2019
CUI: C0376286
Disease: Avitaminosis
Avitaminosis 		disease Nutritional and Metabolic Diseases Disease or Syndrome 17 2 0.010 None 1.000 1 2016 2016
CUI: C1510471
Disease: Vitamin Deficiency
Vitamin Deficiency 		group Nutritional and Metabolic Diseases Disease or Syndrome 17 2 0.010 None 1.000 1 2016 2016
CUI: C0021933
Disease: Intussusception
Intussusception 		disease Digestive System Diseases Disease or Syndrome 19 0.010 None 1.000 1 2018 2018
CUI: C1955760
Disease: Idiopathic normal pressure hydrocephalus (INPH)
Idiopathic normal pressure hydrocephalus (INPH) 		disease Disease or Syndrome 25 0.010 None 1.000 1 2014 2014
CUI: C0038160
Disease: Staphylococcal Infections
Staphylococcal Infections 		group Infections Disease or Syndrome 31 1 0.010 None 1.000 1 2014 2014
CUI: C0040188
Disease: Tic disorder
Tic disorder 		disease Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 31 4 0.010 None 1.000 1 2015 2015
CUI: C0149654
Disease: Conduct Disorder
Conduct Disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 31 10 0.010 None 1.000 1 1 2011 2011
CUI: C0014511
Disease: Epithelial cyst
Epithelial cyst 		phenotype Neoplasms Anatomical Abnormality 32 0.010 None 1.000 1 1997 1997
CUI: C0276548
Disease: HIV encephalitis
HIV encephalitis 		disease Infections; Immune System Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 42 0.010 None 1.000 1 2014 2014
CUI: C0206019
Disease: HIV Encephalopathy
HIV Encephalopathy 		disease Infections; Immune System Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 43 0.010 None 1.000 1 2014 2014
CUI: C0042842
Disease: Vitamin A Deficiency
Vitamin A Deficiency 		disease Nutritional and Metabolic Diseases Disease or Syndrome 44 1 0.010 None 1.000 1 2016 2016
CUI: C0206702
Disease: Klatskin Tumor
Klatskin Tumor 		disease Neoplasms Neoplastic Process 50 0.010 None 1.000 1 2018 2018
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Congenital Abnormality 52 14 0.010 None 1.000 1 2019 2019
CUI: C3714534
Disease: dowling-degos disease
dowling-degos disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 53 7 0.310 None 1.000 1 2013 2013
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
Cerebral Amyloid Angiopathy 		disease Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 60 17 0.010 None 1.000 1 2017 2017
CUI: C3887654
Disease: POLYARTERITIS NODOSA, CHILDHOOD-ONSET
POLYARTERITIS NODOSA, CHILDHOOD-ONSET 		disease Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 63 1 0.010 None 1.000 1 2019 2019
CUI: C0031036
Disease: Polyarteritis Nodosa
Polyarteritis Nodosa 		disease Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 70 0.010 None 1.000 1 2019 2019
CUI: C0033575
Disease: Prostatic Diseases
Prostatic Diseases 		group Male Urogenital Diseases Disease or Syndrome 70 4 0.010 None 1.000 1 2004 2004