SLC29A3, solute carrier family 29 member 3, 55315

N. diseases: 123; N. variants: 21
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.
Diabetes Mellitus, Insulin-Dependent
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 1675 954 0.360 None 1.000 7 2009 2019
CUI: C0020555
Disease: Hypertrichosis
Hypertrichosis
disease Skin and Connective Tissue Diseases Disease or Syndrome 92 27 0.460 None 1.000 7 2009 2019
CUI: C0019625
Disease: Sinus histiocytosis
Sinus histiocytosis
disease Hemic and Lymphatic Diseases Disease or Syndrome 19 2 0.350 None 0.800 5 2010 2013
CUI: C0019618
Disease: Histiocytosis
Histiocytosis
disease Hemic and Lymphatic Diseases Neoplastic Process 32 3 0.440 None 0.750 4 2011 2013
CUI: C0398597
Disease: Histiocytic syndrome
Histiocytic syndrome
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 21 2 0.040 None 0.750 4 2011 2013
CUI: C0432262
Disease: Dysosteosclerosis
Dysosteosclerosis
disease Musculoskeletal Diseases Disease or Syndrome 5 0.330 None 1.000 3 2012 2019
CUI: C0037274
Disease: Dermatologic disorders
Dermatologic disorders
group Skin and Connective Tissue Diseases Disease or Syndrome 617 21 0.030 None 1.000 3 2010 2013
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
group Neoplasms Neoplastic Process 8621 1641 0.020 None 0.500 2 2013 2019
CUI: C4554117
Disease: Diabetes Mellitus, Sudden-Onset
Diabetes Mellitus, Sudden-Onset
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 44 0.300 None 1.000 2 2009 2010
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.020 None 1.000 2 2010 2011
CUI: C3837958
Disease: Diabetes Mellitus, Ketosis-Prone
Diabetes Mellitus, Ketosis-Prone
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 57 4 0.300 None 1.000 2 2009 2010
CUI: C0037277
Disease: Skin Diseases, Genetic
Skin Diseases, Genetic
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 57 6 0.020 None 1.000 2 2012 2014
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
group Neoplasms Neoplastic Process 8221 1374 0.020 None 0.500 2 2013 2019
CUI: C0342302
Disease: Brittle diabetes
Brittle diabetes
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 44 0.300 None 1.000 2 2009 2010
CUI: C0162834
Disease: Hyperpigmentation
Hyperpigmentation
phenotype Skin and Connective Tissue Diseases Pathologic Function 73 11 0.400 None 1.000 2 2009 2010
CUI: C0205734
Disease: Diabetes, Autoimmune
Diabetes, Autoimmune
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 172 4 0.300 None 1.000 2 2009 2010
CUI: C3860213
Disease: Autoinflammatory disorder
Autoinflammatory disorder
disease Disease or Syndrome 60 4 0.310 strong 1.000 2 2012 2013
CUI: C0085078
Disease: Lysosomal Storage Diseases
Lysosomal Storage Diseases
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 130 8 0.010 None 1.000 1 2012 2012
CUI: C0344315
Disease: Depressed mood
Depressed mood
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1461 269 0.010 None 1.000 1 2010 2010
Osteopetrosis, Autosomal Recessive 7
disease Musculoskeletal Diseases; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 2 5 0.010 None 1.000 1 2019 2019
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group Cardiovascular Diseases Disease or Syndrome 2322 1085 0.010 None 1.000 1 2019 2019
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism
disease Endocrine System Diseases Disease or Syndrome 178 18 0.300 None 1.000 1 2010 2010
CUI: C0020619
Disease: Hypogonadism
Hypogonadism
disease Endocrine System Diseases Disease or Syndrome 305 24 0.410 None 1.000 1 2010 2010
Progressive sensorineural hearing impairment
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 78 28 0.010 None 1.000 1 2012 2012
CUI: C0034735
Disease: Raynaud Phenomenon
Raynaud Phenomenon
disease Cardiovascular Diseases Disease or Syndrome 63 1 0.010 None 1.000 1 2015 2015