CASZ1, castor zinc finger 1, 54897

N. diseases: 132; N. variants: 15
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: C1336128
Disease: Stage IB1 Cervical Cancer
Stage IB1 Cervical Cancer
disease Neoplastic Process 1 0.010 None 1.000 1 2019 2019
CUI: C4552926
Disease: Stage IB1 Cervical Cancer AJCC v8
Stage IB1 Cervical Cancer AJCC v8
disease Neoplastic Process 1 0.010 None 1.000 1 2019 2019
CUI: C1842870
Disease: Chromosome 1p36 Deletion Syndrome
Chromosome 1p36 Deletion Syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 6 0.200 None 1.000 1 2014 2014
CUI: C0030442
Disease: Progressive bulbar palsy
Progressive bulbar palsy
disease Nervous System Diseases Disease or Syndrome 10 1 0.010 None 1.000 1 2019 2019
CUI: C0235522
Disease: Disorder of vein
Disorder of vein
group Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 1 2019 2019
CUI: C0270764
Disease: Motor Neuron Disease, Lower
Motor Neuron Disease, Lower
disease Nervous System Diseases Disease or Syndrome 23 7 0.010 None 1.000 1 2018 2018
Metastatic Malignant Neoplasm to the Leptomeninges
disease Nervous System Diseases Neoplastic Process 25 9 0.010 None 1.000 1 2019 2019
CUI: C2931826
Disease: Potassium aggravated myotonia
Potassium aggravated myotonia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 27 18 0.010 None 1.000 1 2017 2017
CUI: C0030360
Disease: Papillon-Lefevre Disease
Papillon-Lefevre Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 29 19 0.010 None 1.000 1 2018 2018
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 30 32 0.100 None 1.000 1 1 2019 2019
Diastolic blood pressure measurement
phenotype Diagnostic Procedure 35 81 0.100 None 1.000 1 1 2018 2018
CUI: C0003028
Disease: Anhidrosis
Anhidrosis
disease Skin and Connective Tissue Diseases Disease or Syndrome 37 2 0.010 None 1.000 1 1986 1986
Left ventricular noncompaction cardiomyopathy
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 39 28 0.010 None 1.000 1 2019 2019
CUI: C1609524
Disease: ADHF
ADHF
disease Disease or Syndrome 46 0.010 None 1.000 1 2019 2019
CUI: C0857175
Disease: Postinfarction
Postinfarction
disease Disease or Syndrome 49 1 0.010 None 1.000 1 2017 2017
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement
phenotype Diagnostic Procedure 54 95 0.100 None 1.000 1 1 2018 2018
Deficiency of glucose-6-phosphate dehydrogenase
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 75 20 0.010 None 1.000 1 2009 2009
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE
phenotype Finding 80 134 0.100 None 1.000 1 1 2019 2019
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
disease Cardiovascular Diseases Disease or Syndrome 83 47 0.010 None 1.000 1 2017 2017
CUI: C0730285
Disease: Diabetic macular edema
Diabetic macular edema
disease Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 92 6 0.010 None 1.000 1 2018 2018
CUI: C0034885
Disease: Rectal Neoplasms
Rectal Neoplasms
group Digestive System Diseases; Neoplasms Neoplastic Process 93 21 0.010 None 1.000 1 2017 2017
CUI: C0033141
Disease: Cardiomyopathies, Primary
Cardiomyopathies, Primary
group Cardiovascular Diseases Disease or Syndrome 108 1 0.010 None 1.000 1 2017 2017
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
phenotype Organism Function 109 220 0.100 None 1.000 1 1 2011 2011
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 130 1012 0.010 None 1.000 1 2018 2018
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
phenotype Finding 146 344 0.100 None 1.000 4 3 2016 2018