BGLAP, bone gamma-carboxyglutamate protein, 632

N. diseases: 274; N. variants: 2
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: C0028259
Disease: Nodule
Nodule
phenotype Acquired Abnormality 278 19 0.080 None 1.000 8 2013 2019
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
phenotype Disease or Syndrome 716 25 0.030 None 1.000 3 2018 2019
CUI: C1739135
Disease: Progression of prostate cancer
Progression of prostate cancer
disease Neoplastic Process 398 7 0.020 None 1.000 2 2003 2009
CUI: C3665629
Disease: Dental fluorosis
Dental fluorosis
disease Congenital Abnormality 24 3 0.020 None 1.000 2 2009 2012
CUI: C0221106
Disease: Alkalemia
Alkalemia
disease Disease or Syndrome 38 0.010 None 1.000 1 2019 2019
CUI: C0259779
Disease: Fibrous Dysplasia
Fibrous Dysplasia
disease Congenital Abnormality 53 5 0.010 None 1.000 1 2007 2007
CUI: C0853241
Disease: Exacerbation of anxiety
Exacerbation of anxiety
phenotype Sign or Symptom 1 0.010 None 1.000 1 2018 2018
CUI: C1265884
Disease: Eggshell calcium deposition
Eggshell calcium deposition
disease Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.010 None 1.000 1 2007 2007
Metastasis from malignant tumor of prostate
disease Neoplastic Process 342 18 0.010 None 1.000 1 2000 2000
Hepatitis B Virus-Related Hepatocellular Carcinoma
disease Neoplastic Process 76 8 0.010 None 1.000 1 2015 2015
CUI: C1561826
Disease: Overweight and obesity
Overweight and obesity
disease Disease or Syndrome 81 29 0.010 None 1.000 1 2015 2015
androgen independent prostate cancer
disease Neoplastic Process 190 5 0.010 None 1.000 1 2005 2005
Brachytelephalangic Chondrodysplasia Punctata
disease Disease or Syndrome 7 11 0.010 None 1.000 1 1989 1989
CUI: C2826323
Disease: Refractory Cytopenia of Childhood
Refractory Cytopenia of Childhood
disease Neoplastic Process 264 3 0.010 None 1.000 1 2010 2010
CUI: C2874202
Disease: Constitutional delay of puberty
Constitutional delay of puberty
disease Disease or Syndrome 4 3 0.010 None 1.000 1 2017 2017
CUI: C3554225
Disease: LEPTIN RECEPTOR DEFICIENCY
LEPTIN RECEPTOR DEFICIENCY
disease Disease or Syndrome 9 3 0.010 None 1.000 1 2017 2017
CUI: C3715128
Disease: HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
disease Disease or Syndrome 5 22 0.200 None 1.000 1 1990 1990
CUI: C3825201
Disease: Mitochondrial pathology
Mitochondrial pathology
phenotype Disease or Syndrome 20 6 0.010 None 1.000 1 2017 2017
CUI: C3888204
Disease: ACTN3 DEFICIENCY
ACTN3 DEFICIENCY
disease Disease or Syndrome 4 1 0.010 None 1.000 1 2017 2017
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system
disease Anatomical Abnormality 148 18 0.010 None 1.000 1 2018 2018
Obstructive sleep apnea hypopnea syndrome
disease Disease or Syndrome 41 7 0.010 None 1.000 1 2017 2017
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME
disease Disease or Syndrome 5 0.200 None 1.000 1 1990 1990
Metastatic castration-resistant prostate cancer
disease Neoplastic Process 140 2 0.010 None 1.000 1 2003 2003
CUI: C0011570
Disease: Mental Depression
Mental Depression
disease Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1478 271 0.010 None 1.000 1 2018 2018