GNA11, G protein subunit alpha 11, 2767

N. diseases: 122; N. variants: 9
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: C4725091
Disease: metastatic intraocular melanoma
metastatic intraocular melanoma 		disease Neoplasms; Eye Diseases Neoplastic Process 53 0.010 None 1.000 1 2018 2018
CUI: C3899655
Disease: Childhood Langerhans Cell Histiocytosis
Childhood Langerhans Cell Histiocytosis 		disease Respiratory Tract Diseases; Hemic and Lymphatic Diseases Neoplastic Process 40 2 0.010 None 1.000 1 2018 2018
CUI: C0878675
Disease: Erdheim-Chester Disease
Erdheim-Chester Disease 		disease Hemic and Lymphatic Diseases Disease or Syndrome 29 2 0.010 None 1.000 1 2018 2018
CUI: C3809243
Disease: HYPOCALCEMIA, AUTOSOMAL DOMINANT 2
HYPOCALCEMIA, AUTOSOMAL DOMINANT 2 		disease Disease or Syndrome 1 5 0.800 strong 1.000 4 5 2013 2017
CUI: C0346373
Disease: Malignant melanoma of iris
Malignant melanoma of iris 		disease Neoplasms; Eye Diseases Neoplastic Process 10 1 0.410 None 1.000 3 2010 2017
CUI: C0221002
Disease: Hyperparathyroidism, Primary
Hyperparathyroidism, Primary 		disease Endocrine System Diseases Disease or Syndrome 115 39 0.130 None 1.000 3 1993 2017
CUI: C0334431
Disease: Melanocytoma
Melanocytoma 		disease Neoplastic Process 18 3 0.020 None 1.000 2 2013 2017
CUI: C0334447
Disease: Malignant blue nevus of skin
Malignant blue nevus of skin 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 7 1 0.020 None 1.000 2 1 2016 2017
CUI: C0020502
Disease: Hyperparathyroidism
Hyperparathyroidism 		disease Endocrine System Diseases Disease or Syndrome 111 14 0.020 None 1.000 2 2015 2017
CUI: C0271846
Disease: Familial hyperparathyroidism
Familial hyperparathyroidism 		disease Endocrine System Diseases Disease or Syndrome 7 1 0.010 None 1.000 1 2017 2017
CUI: C1832648
Disease: Hypoparathyroidism familial isolated
Hypoparathyroidism familial isolated 		disease Endocrine System Diseases Disease or Syndrome 8 8 0.010 None < 0.001 1 2017 2017
CUI: C0020626
Disease: Hypoparathyroidism
Hypoparathyroidism 		disease Endocrine System Diseases Disease or Syndrome 92 15 0.010 None 1.000 1 2017 2017
CUI: C1306247
Disease: Melanotic neurilemmoma
Melanotic neurilemmoma 		disease Neoplasms; Nervous System Diseases; Otorhinolaryngologic Diseases Neoplastic Process 3 0.010 None 1.000 1 2017 2017
CUI: C0340803
Disease: Capillary malformation (disorder)
Capillary malformation (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 40 13 0.010 None 1.000 1 2017 2017
CUI: C0406810
Disease: Carney Complex
Carney Complex 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Cardiovascular Diseases Disease or Syndrome 82 27 0.010 None 1.000 1 2017 2017
CUI: C1332347
Disease: Atypical Ductal Breast Hyperplasia
Atypical Ductal Breast Hyperplasia 		disease Neoplasms Neoplastic Process 80 17 0.040 None 1.000 4 2014 2016
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia 		phenotype Nutritional and Metabolic Diseases Disease or Syndrome 94 13 0.140 None 1.000 4 2 1980 2016
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 507 248 0.430 None 1.000 4 1 2014 2016
CUI: C1840347
Disease: HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder)
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder) 		disease Nutritional and Metabolic Diseases Disease or Syndrome 1 2 0.700 strong 1.000 3 2 2013 2016
CUI: C0332977
Disease: Congenital hemangiomatosis
Congenital hemangiomatosis 		disease Congenital Abnormality 1 0.010 None 1.000 1 2016 2016
CUI: C3839296
Disease: Phakomatosis cesiomarmorata
Phakomatosis cesiomarmorata 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Nervous System Diseases Congenital Abnormality 1 0.300 None 1.000 1 2016 2016
CUI: C3838883
Disease: Phakomatosis cesioflammea
Phakomatosis cesioflammea 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Nervous System Diseases Congenital Abnormality 2 0.300 None 1.000 1 2016 2016
CUI: C3898222
Disease: mucosal melanoma
mucosal melanoma 		disease Neoplastic Process 24 1 0.010 None 1.000 1 2016 2016
CUI: C0235753
Disease: Congenital hemangioma
Congenital hemangioma 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases Neoplastic Process 5 0.310 moderate 1.000 1 2016 2016
CUI: C0494165
Disease: Secondary malignant neoplasm of liver
Secondary malignant neoplasm of liver 		disease Digestive System Diseases; Neoplasms Neoplastic Process 951 34 0.010 None 1.000 1 1 2016 2016