WNK1, WNK lysine deficient protein kinase 1, 65125

N. diseases: 460; N. variants: 26
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: C1840391
Disease: Pseudohypoaldosteronism, Type IIc
Pseudohypoaldosteronism, Type IIc 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 1 2 0.600 None 1.000 3 2 2001 2005
CUI: C2752089
Disease: Neuropathy, Hereditary Sensory And Autonomic, Type IIA
Neuropathy, Hereditary Sensory And Autonomic, Type IIA 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 5 28 0.600 None 1.000 5 6 2001 2006
CUI: C0302360
Disease: Disease caused by Shigella boydii
Disease caused by Shigella boydii 		disease Digestive System Diseases; Infections Disease or Syndrome 5 0.010 None 1.000 1 2010 2010
CUI: C1394254
Disease: Cryptitis
Cryptitis 		disease Disease or Syndrome 5 0.010 None 1.000 1 2009 2009
CUI: C4289581
Disease: RELA fusion-positive ependymoma
RELA fusion-positive ependymoma 		disease Neoplasms Neoplastic Process 6 0.010 None 1.000 1 2019 2019
CUI: C0151934
Disease: Hypogeusia
Hypogeusia 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 6 0.100 None 0
CUI: C4025744
Disease: Foot acroosteolysis
Foot acroosteolysis 		phenotype Pathologic Function 6 0.100 None 0
CUI: C0020072
Disease: Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 8 9 0.200 None 0.929 14 3 2004 2018
CUI: C1837602
Disease: Painless fractures due to injury
Painless fractures due to injury 		phenotype Finding 8 0.100 None 0
CUI: C1852289
Disease: Autoamputation of digits
Autoamputation of digits 		phenotype Musculoskeletal Diseases Finding 8 0.100 None 0
CUI: C1969073
Disease: Hyperchloremic metabolic acidosis
Hyperchloremic metabolic acidosis 		phenotype Disease or Syndrome 8 0.100 None 0
CUI: C4732740
Disease: Acral ulceration
Acral ulceration 		phenotype Finding 8 0.100 None 0
CUI: C0006285
Disease: Bronchopneumonia
Bronchopneumonia 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 9 0.010 None 1.000 1 2008 2008
CUI: C0154652
Disease: Eosinophilic meningitis
Eosinophilic meningitis 		disease Nervous System Diseases Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C1449843
Disease: Pseudohypoaldosteronism, Type I, Autosomal Recessive
Pseudohypoaldosteronism, Type I, Autosomal Recessive 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 10 6 0.300 None 1.000 1 2012 2012
CUI: C2713447
Disease: Hyperpotassemia and Hypertension, Familial
Hyperpotassemia and Hypertension, Familial 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 10 0.300 None 1.000 1 2012 2012
CUI: C4727578
Disease: Locally Advanced Squamous Cell Carcinoma
Locally Advanced Squamous Cell Carcinoma 		disease Neoplastic Process 10 0.010 None 1.000 1 2015 2015
CUI: C4025676
Disease: Abnormality of the knee
Abnormality of the knee 		disease Anatomical Abnormality 10 0.100 None 0
CUI: C0275904
Disease: Tuberculosis, Central Nervous System
Tuberculosis, Central Nervous System 		disease Infections; Nervous System Diseases Disease or Syndrome 11 0.010 None 1.000 1 2010 2010
CUI: C0030578
Disease: Paronychia Inflammation
Paronychia Inflammation 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 11 0.100 None 0
CUI: C0085679
Disease: Hyperchloremia
Hyperchloremia 		disease Nutritional and Metabolic Diseases Disease or Syndrome 12 2 0.100 None 0
CUI: C3469605
Disease: PSEUDOHYPOALDOSTERONISM, TYPE IID
PSEUDOHYPOALDOSTERONISM, TYPE IID 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 13 29 0.080 None 1.000 8 2007 2019
CUI: C1449842
Disease: Pseudohypoaldosteronism, Type I, Autosomal Dominant
Pseudohypoaldosteronism, Type I, Autosomal Dominant 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 13 20 0.300 None 1.000 1 2012 2012
CUI: C0032827
Disease: Potassium Deficiency
Potassium Deficiency 		disease Nutritional and Metabolic Diseases Disease or Syndrome 14 0.020 None 1.000 2 2008 2017
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 14 0.010 None 1.000 1 2009 2009