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: C0020502
Disease: Hyperparathyroidism
Hyperparathyroidism
disease Endocrine System Diseases Disease or Syndrome 111 14 0.020 None 1.000 2 2015 2017
HYPERPARATHYROIDISM, NEONATAL SEVERE
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases Disease or Syndrome 14 14 0.020 None 1.000 2 1998 2004
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: C0085681
Disease: Hyperphosphatemia (disorder)
Hyperphosphatemia (disorder)
disease Nutritional and Metabolic Diseases Disease or Syndrome 65 1 0.100 None 0
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: C3715128
Disease: HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
disease Disease or Syndrome 5 22 0.300 None 1.000 1 2013 2013
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME
disease Disease or Syndrome 5 0.300 None 1.000 1 2013 2013
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: C0020599
Disease: Hypocalciuria
Hypocalciuria
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 16 4 0.100 None 0
CUI: C3875492
Disease: Hypocalciuric hypercalcemia
Hypocalciuric hypercalcemia
disease Nutritional and Metabolic Diseases Disease or Syndrome 5 0.010 None 1.000 1 1998 1998
Hypocalciuric hypercalcemia, familial, type 1
disease Nutritional and Metabolic Diseases Disease or Syndrome 46 58 0.100 None 1.000 11 1 2010 2018
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: C0151723
Disease: Hypomagnesemia
Hypomagnesemia
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 58 11 0.100 None 0
CUI: C4552839
Disease: Hypomagnesemia, CTCAE
Hypomagnesemia, CTCAE
phenotype Finding 21 0.100 None 0
CUI: C0020626
Disease: Hypoparathyroidism
Hypoparathyroidism
disease Endocrine System Diseases Disease or Syndrome 92 15 0.010 None 1.000 1 2017 2017
Hypoparathyroidism familial isolated
disease Endocrine System Diseases Disease or Syndrome 8 8 0.010 None < 0.001 1 2017 2017
CUI: C0020649
Disease: Hypotension
Hypotension
phenotype Cardiovascular Diseases Finding 125 2 0.100 None 0
CUI: C2036842
Disease: Inferior lens subluxation
Inferior lens subluxation
disease Eye Diseases Disease or Syndrome 5 0.100 None 0
CUI: C4020969
Disease: Inflammatory abnormality of the eye
Inflammatory abnormality of the eye
disease Disease or Syndrome 88 1 0.100 None 0
CUI: C0151740
Disease: Intracranial Hypertension
Intracranial Hypertension
disease Nervous System Diseases Finding 72 1 0.100 None 0
CUI: C1860236
Disease: Irregular hyperpigmentation
Irregular hyperpigmentation
phenotype Skin and Connective Tissue Diseases Finding 55 2 0.100 None 0
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: 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: C0346379
Disease: Malignant melanoma of ciliary body
Malignant melanoma of ciliary body
disease Neoplasms; Eye Diseases Neoplastic Process 6 0.100 None 0
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