PRKCD, protein kinase C delta, 5580

N. diseases: 287; N. variants: 4
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: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		phenotype Organism Function 45 84 0.100 None 1.000 1 1 2018 2018
CUI: C0392171
Disease: Influenza-like symptoms
Influenza-like symptoms 		phenotype Sign or Symptom 30 4 0.010 None 1.000 1 2010 2010
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		phenotype Neoplastic Process 6626 169 0.010 None 1.000 1 2011 2011
CUI: C1397307
Disease: Cardiac fibrosis
Cardiac fibrosis 		disease Disease or Syndrome 297 3 0.010 None 1.000 1 2018 2018
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		disease Finding 578 1158 0.100 None 1.000 1 1 2018 2018
CUI: C2062441
Disease: Influenza A
Influenza A 		disease Disease or Syndrome 563 19 0.010 None 1.000 1 2009 2009
CUI: C3280742
Disease: SYSTEMIC LUPUS ERYTHEMATOSUS 16
SYSTEMIC LUPUS ERYTHEMATOSUS 16 		disease Disease or Syndrome 5 0.300 None 1.000 1 2013 2013
CUI: C3642347
Disease: Basal-Like Breast Carcinoma
Basal-Like Breast Carcinoma 		disease Neoplastic Process 245 9 0.010 None 1.000 1 2015 2015
CUI: C3809928
Disease: AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III 		disease Disease or Syndrome 1 0.500 strong 1.000 1 2013 2013
CUI: C4733227
Disease: ovarian papillary serous carcinoma
ovarian papillary serous carcinoma 		disease Neoplastic Process 9 0.010 None 1.000 1 2014 2014
CUI: C0151379
Disease: Rheumatoid factor positive (finding)
Rheumatoid factor positive (finding) 		phenotype Laboratory or Test Result 7 0.100 None 0
CUI: C1848389
Disease: Posterior pharyngeal cleft
Posterior pharyngeal cleft 		phenotype Finding 12 0.100 None 0
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase 		phenotype Finding 212 9 0.100 None 0
CUI: C1855710
Disease: Bone marrow hypocellularity
Bone marrow hypocellularity 		phenotype Finding 64 5 0.100 None 0
CUI: C1858973
Disease: Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells
Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells 		phenotype Finding 5 0.100 None 0
CUI: C1858981
Disease: Antineutrophil antibody positivity
Antineutrophil antibody positivity 		phenotype Laboratory or Test Result 15 0.100 None 0
CUI: C1860320
Disease: Bone marrow hypercellularity
Bone marrow hypercellularity 		phenotype Finding 26 0.100 None 0
CUI: C1867873
Disease: Failure to thrive in infancy
Failure to thrive in infancy 		phenotype Finding 97 12 0.100 None 0
CUI: C3277226
Disease: Restrictive ventilatory defect
Restrictive ventilatory defect 		phenotype Finding 61 8 0.100 None 0
CUI: C4019436
Disease: Antiphospholipid antibody positivity
Antiphospholipid antibody positivity 		phenotype Finding 18 0.100 None 0
CUI: C4021032
Disease: Abnormal vitamin B12 level
Abnormal vitamin B12 level 		phenotype Finding 5 0.100 None 0
CUI: C4021747
Disease: Specific anti-polysaccharide antibody deficiency
Specific anti-polysaccharide antibody deficiency 		phenotype Finding 6 0.100 None 0
CUI: C4048270
Disease: Decreased antibody level in blood
Decreased antibody level in blood 		phenotype Finding 75 5 0.100 None 0
CUI: C4280772
Disease: Abnormal serum interleukin level
Abnormal serum interleukin level 		phenotype Finding 6 0.100 None 0
CUI: C4531155
Disease: Abnormal proportion of CD8 T cells
Abnormal proportion of CD8 T cells 		phenotype Finding 6 0.100 None 0