SLC30A10, solute carrier family 30 member 10, 55532

N. diseases: 120; N. variants: 22
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: C2931689
Disease: Dystrophia myotonica 2
Dystrophia myotonica 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 118 21 0.020 None 1.000 2 2008 2017
CUI: C0025958
Disease: Microcephaly
Microcephaly
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Congenital Abnormality 1064 27 0.100 None 0
CUI: C3272841
Disease: MUTYH-Associate Polyposis
MUTYH-Associate Polyposis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms Neoplastic Process 73 36 0.010 None 1.000 1 2017 2017
CUI: C0268559
Disease: Hyperglycinemia
Hyperglycinemia
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 14 0.100 None 0
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 384 698 0.010 None 1.000 1 2016 2016
CUI: C0008370
Disease: Cholestasis
Cholestasis
disease Digestive System Diseases Disease or Syndrome 420 15 0.300 None 1.000 1 2016 2016
CUI: C0017154
Disease: Gastritis, Atrophic
Gastritis, Atrophic
disease Digestive System Diseases Disease or Syndrome 203 61 0.010 None 1.000 1 2016 2016
CUI: C0341439
Disease: Chronic liver disease
Chronic liver disease
group Digestive System Diseases Disease or Syndrome 196 14 0.010 None 1.000 1 2016 2016
CUI: C3887639
Disease: Autoimmune gastritis
Autoimmune gastritis
disease Digestive System Diseases Disease or Syndrome 28 1 0.010 None 1.000 1 2015 2015
CUI: C0014867
Disease: Esophageal Varices
Esophageal Varices
disease Digestive System Diseases Disease or Syndrome 56 5 0.100 None 0
CUI: C0020541
Disease: Portal Hypertension
Portal Hypertension
disease Digestive System Diseases Disease or Syndrome 167 9 0.100 None 0
CUI: C0021670
Disease: insulinoma
insulinoma
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 258 8 0.040 None 1.000 4 2010 2019
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 527 263 0.010 None 1.000 1 2016 2016
CUI: C0011847
Disease: Diabetes
Diabetes
disease Endocrine System Diseases Disease or Syndrome 2359 710 0.100 None 0.970 33 2008 2019
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction
phenotype Endocrine System Diseases Disease or Syndrome 90 10 0.010 None 1.000 1 2015 2015
CUI: C0020595
Disease: Hypoaldosteronism
Hypoaldosteronism
disease Endocrine System Diseases Disease or Syndrome 18 0.010 None 1.000 1 2015 2015
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
disease Endocrine System Diseases Disease or Syndrome 613 283 0.310 None 1.000 1 2017 2017
CUI: C0271791
Disease: Severe hypothyroidism
Severe hypothyroidism
disease Endocrine System Diseases Disease or Syndrome 9 2 0.010 None 1.000 1 2017 2017
CUI: C0271801
Disease: Central hypothyroidism
Central hypothyroidism
disease Endocrine System Diseases Disease or Syndrome 35 3 0.300 None 1.000 1 2017 2017
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism
disease Endocrine System Diseases Disease or Syndrome 47 2 0.300 None 1.000 1 2017 2017
CUI: C4316995
Disease: Primary Hypothyroidism
Primary Hypothyroidism
disease Endocrine System Diseases Disease or Syndrome 19 3 0.300 None 1.000 1 2017 2017
CUI: C0027092
Disease: Myopia
Myopia
disease Eye Diseases Disease or Syndrome 490 167 0.010 None 1.000 1 2012 2012
CUI: C0018213
Disease: Graves Disease
Graves Disease
disease Eye Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 585 352 0.010 None 1.000 1 2019 2019
CUI: C0032461
Disease: Polycythemia
Polycythemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 82 22 0.420 None 1.000 3 2012 2019
CUI: C1527405
Disease: Erythrocytosis
Erythrocytosis
phenotype Hemic and Lymphatic Diseases Finding 9 1 0.300 None 1.000 1 2012 2012