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: C0220633
Disease: Uveal melanoma
Uveal melanoma
disease Neoplasms; Eye Diseases Neoplastic Process 376 22 0.800 None 0.977 44 1 2010 2019
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: C0025202
Disease: melanoma
melanoma
disease Neoplasms Neoplastic Process 3087 515 0.700 None 1.000 26 1 1989 2019
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: 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: 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: C0346388
Disease: Malignant melanoma of choroid
Malignant melanoma of choroid
disease Neoplasms; Eye Diseases Neoplastic Process 27 5 0.400 None 1.000 2 2010 2013
CUI: C4048195
Disease: Autosomal dominant hypocalcemia
Autosomal dominant hypocalcemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 29 9 0.330 None 1.000 3 2 2013 2020
Port-wine stain with oculocutaneous melanosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Nervous System Diseases Congenital Abnormality 3 0.320 None 1.000 2 2016 2019
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
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME
disease Disease or Syndrome 5 0.300 None 1.000 1 2013 2013
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: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 406 58 0.300 None 1.000 1 1998 1998
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: C3715128
Disease: HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
disease Disease or Syndrome 5 22 0.300 None 1.000 1 2013 2013
CUI: C0020437
Disease: Hypercalcemia
Hypercalcemia
disease Nutritional and Metabolic Diseases Disease or Syndrome 157 9 0.150 None 1.000 5 1980 2018
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: C0221002
Disease: Hyperparathyroidism, Primary
Hyperparathyroidism, Primary
disease Endocrine System Diseases Disease or Syndrome 115 39 0.130 None 1.000 3 1993 2017
Hypocalciuric hypercalcemia, familial, type 1
disease Nutritional and Metabolic Diseases Disease or Syndrome 46 58 0.100 None 1.000 11 1 2010 2018
CUI: C0027651
Disease: Neoplasms
Neoplasms
group Neoplasms Neoplastic Process 10161 1644 0.100 None 0.900 10 1 2012 2018
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
phenotype Clinical Attribute 843 1931 0.100 None 1.000 1 1 2019 2019
CUI: C3698239
Disease: Cerebral cortex myoclonus
Cerebral cortex myoclonus
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 14 1 0.100 None 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Finding 115 6 0.100 None 0
CUI: C0266537
Disease: Congenital lamellar cataract
Congenital lamellar cataract
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 18 6 0.100 None 0
CUI: C0037763
Disease: Spasm
Spasm
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 172 9 0.100 None 0