LDHA, lactate dehydrogenase A, 3939

N. diseases: 185; N. variants: 0
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.
Lactate dehydrogenase deficiency type A
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 1 0.600 strong 1.000 3 1984 2016
CUI: C0334477
Disease: Cellular leiomyoma
Cellular leiomyoma
disease Neoplasms; Musculoskeletal Diseases Neoplastic Process 5 0.010 None 1.000 1 2018 2018
CUI: C4684861
Disease: Recurrent Malignant Glioma
Recurrent Malignant Glioma
disease Neoplasms Neoplastic Process 13 0.010 None 1.000 1 2018 2018
CUI: C0027080
Disease: Myoglobinuria
Myoglobinuria
phenotype Musculoskeletal Diseases Finding 17 1 0.400 None 1.000 1 2011 2011
CUI: C0152081
Disease: Pustular psoriasis
Pustular psoriasis
disease Skin and Connective Tissue Diseases Disease or Syndrome 18 1 0.010 None 1.000 1 2016 2016
CUI: C0338113
Disease: Uterine Corpus Sarcoma
Uterine Corpus Sarcoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 30 0.010 None 1.000 1 2018 2018
CUI: C0035410
Disease: Rhabdomyolysis
Rhabdomyolysis
phenotype Musculoskeletal Diseases Pathologic Function 36 15 0.100 None 0
CUI: C1849488
Disease: Increased serum pyruvate
Increased serum pyruvate
phenotype Finding 45 1 0.100 None 0
Hereditary Leiomyomatosis and Renal Cell Cancer
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases Neoplastic Process 61 59 0.010 None 1.000 1 2009 2009
CUI: C0017919
Disease: Glycogen Storage Disease
Glycogen Storage Disease
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 63 16 0.300 strong 1.000 2 1984 2016
CUI: C2004489
Disease: Regurgitation
Regurgitation
phenotype Sign or Symptom 66 0.010 None 1.000 1 1993 1993
CUI: C0424551
Disease: Impaired exercise tolerance
Impaired exercise tolerance
phenotype Finding 76 7 0.100 None 0
CUI: C0030186
Disease: Paget Disease Extramammary
Paget Disease Extramammary
disease Neoplasms Neoplastic Process 79 1 0.010 None 1.000 1 2019 2019
CUI: C0221170
Disease: Muscular stiffness
Muscular stiffness
phenotype Nervous System Diseases Sign or Symptom 92 6 0.110 None < 0.001 1 1988 1988
CUI: C0027659
Disease: Neoplasms, Experimental
Neoplasms, Experimental
phenotype Neoplasms Neoplastic Process; Experimental Model of Disease 95 0.200 None 1.000 1 2000 2000
CUI: C0036529
Disease: Myocardial Diseases, Secondary
Myocardial Diseases, Secondary
group Cardiovascular Diseases Disease or Syndrome 101 0.300 None 1.000 1 2004 2004
CUI: C1378050
Disease: Oncocytic Neoplasm
Oncocytic Neoplasm
disease Neoplastic Process 105 2 0.010 None 1.000 1 2018 2018
CUI: C0033141
Disease: Cardiomyopathies, Primary
Cardiomyopathies, Primary
group Cardiovascular Diseases Disease or Syndrome 108 1 0.300 None 1.000 1 2004 2004
CUI: C1510502
Disease: Oxyphilic Adenoma
Oxyphilic Adenoma
disease Neoplasms Neoplastic Process 114 3 0.010 None 1.000 1 2018 2018
CUI: C1851710
Disease: LATERAL MENINGOCELE SYNDROME
LATERAL MENINGOCELE SYNDROME
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 118 12 0.010 None 1.000 1 2018 2018
CUI: C1863753
Disease: LIMB-MAMMARY SYNDROME
LIMB-MAMMARY SYNDROME
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 120 1 0.010 None 1.000 1 2018 2018
CUI: C1839259
Disease: Bulbo-Spinal Atrophy, X-Linked
Bulbo-Spinal Atrophy, X-Linked
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 126 30 0.010 None 1.000 1 2018 2018
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 140 72 0.010 None 1.000 1 2018 2018
Metastatic castration-resistant prostate cancer
disease Neoplastic Process 140 2 0.010 None 1.000 1 2019 2019
CUI: C0018021
Disease: Goiter
Goiter
phenotype Endocrine System Diseases Disease or Syndrome 142 19 0.010 None 1.000 1 2015 2015