MYOCD, myocardin, 93649

N. diseases: 79; N. variants: 7
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: C2747862
Disease: Hysteromyoma
Hysteromyoma
disease Neoplastic Process 2 0.010 None 1.000 1 2018 2018
CUI: C0549253
Disease: Dilatation of the bladder
Dilatation of the bladder
phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases Finding 3 1 0.300 strong 1.000 1 2019 2019
CUI: C0021308
Disease: Infarction
Infarction
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 15 0.010 None 1.000 1 2007 2007
CUI: C2242703
Disease: Cardio-Renal Syndrome
Cardio-Renal Syndrome
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome 21 0.010 None 1.000 1 2019 2019
Undifferentiated (Embryonal) Sarcoma
disease Neoplastic Process 35 4 0.010 None 1.000 1 2009 2009
Dementia due to Alzheimer's disease (disorder)
disease Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 35 1 0.010 None 1.000 1 2007 2007
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval
phenotype Finding 57 138 0.100 None 1.000 2 2 2018 2019
CUI: C0018794
Disease: Heart Block
Heart Block
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 58 7 0.010 None 1.000 1 2007 2007
CUI: C0340279
Disease: Ventricular hypertrophy
Ventricular hypertrophy
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 60 9 0.010 None 1.000 1 2018 2018
CUI: C3178782
Disease: Aortic Stiffness
Aortic Stiffness
phenotype Disease or Syndrome 61 11 0.020 None 1.000 2 2017 2017
CUI: C3888088
Disease: SMITH-MCCORT DYSPLASIA 1
SMITH-MCCORT DYSPLASIA 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 62 3 0.020 None 1.000 2 2012 2017
Hypertrophic disorder of skin, unspecified
group Skin and Connective Tissue Diseases Disease or Syndrome 62 1 0.010 None 1.000 1 2006 2006
CUI: C0524662
Disease: Opiate Addiction
Opiate Addiction
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 81 46 0.010 None 1.000 1 2010 2010
CUI: C0079680
Disease: Lentivirus Infections
Lentivirus Infections
group Infections Disease or Syndrome 88 0.010 None 1.000 1 2018 2018
CUI: C1383860
Disease: Cardiac Hypertrophy
Cardiac Hypertrophy
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 88 11 0.300 None 1.000 1 2006 2006
CUI: C0041948
Disease: Uremia
Uremia
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 110 2 0.010 None 1.000 1 2017 2017
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 0.030 None 1.000 3 2009 2016
CUI: C1863753
Disease: LIMB-MAMMARY SYNDROME
LIMB-MAMMARY SYNDROME
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 120 1 0.030 None 1.000 3 2009 2016
CUI: C0279986
Disease: Childhood Leiomyosarcoma
Childhood Leiomyosarcoma
disease Neoplasms Neoplastic Process 140 1 0.010 None 1.000 1 2010 2010
CUI: C0278607
Disease: Adult Leiomyosarcoma
Adult Leiomyosarcoma
disease Neoplasms Neoplastic Process 141 1 0.010 None 1.000 1 2010 2010
CUI: C0278608
Disease: Adult Liposarcoma
Adult Liposarcoma
disease Neoplasms Neoplastic Process 143 6 0.010 None 1.000 1 2009 2009
CUI: C0279984
Disease: Childhood Liposarcoma
Childhood Liposarcoma
disease Neoplasms Neoplastic Process 143 6 0.010 None 1.000 1 2009 2009
CUI: C0334463
Disease: Malignant Fibrous Histiocytoma
Malignant Fibrous Histiocytoma
disease Neoplasms Neoplastic Process 150 3 0.010 None 1.000 1 2014 2014
CUI: C2585653
Disease: Persistent atrial fibrillation
Persistent atrial fibrillation
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 156 0.300 None 1.000 2 2018 2018
CUI: C3468561
Disease: familial atrial fibrillation
familial atrial fibrillation
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 157 1 0.300 None 1.000 2 2018 2018