CREBBP, CREB binding protein, 1387

N. diseases: 438; N. variants: 123
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: C0432072
Disease: Dysmorphic features
Dysmorphic features
disease Congenital Abnormality 439 617 0.100 None 1.000 18 4 1963 2017
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.060 None 1.000 6 2011 2019
Treatment related acute myeloid leukaemia
disease Neoplastic Process 65 4 0.060 None 1.000 6 1997 2012
CUI: C0302486
Disease: Erythrophagocytosis
Erythrophagocytosis
disease Disease or Syndrome 40 0.030 None 1.000 3 1998 2014
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
disease Neoplastic Process 860 154 0.030 None 1.000 3 2000 2017
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
phenotype Neoplastic Process 1027 20 0.030 None 1.000 3 2002 2019
CUI: C1855496
Disease: Contiguous gene syndrome
Contiguous gene syndrome
disease Disease or Syndrome 52 0.020 None 1.000 2 2007 2015
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system
disease Anatomical Abnormality 148 18 0.020 None 1.000 2 1999 2004
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
disease Neoplastic Process 2 0.300 None 1.000 2 2008 2013
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.020 None 1.000 2 2007 2017
CUI: C0039147
Disease: Syrinx formation
Syrinx formation
disease Anatomical Abnormality 18 0.010 None 1.000 1 2011 2011
CUI: C0240310
Disease: Hypoplasia of the maxilla
Hypoplasia of the maxilla
disease Congenital Abnormality 113 5 0.110 None 1.000 1 1999 1999
CUI: C0280141
Disease: Acute Undifferentiated Leukemia
Acute Undifferentiated Leukemia
disease Neoplastic Process 119 1 0.010 None 1.000 1 2010 2010
CUI: C0376705
Disease: Viral Load result
Viral Load result
phenotype Finding 65 91 0.100 None 1.000 1 1 2019 2019
QT interval feature (observable entity)
phenotype Clinical Attribute 75 226 0.100 None 1.000 1 1 2014 2014
CUI: C0431369
Disease: Dysgenesis of corpus callosum
Dysgenesis of corpus callosum
disease Congenital Abnormality 25 3 0.010 None 1.000 1 2010 2010
CUI: C0558920
Disease: Lump on thigh
Lump on thigh
phenotype Sign or Symptom 6 0.010 None 1.000 1 2017 2017
CUI: C0741899
Disease: Poorly differentiated carcinoma
Poorly differentiated carcinoma
phenotype Neoplastic Process 64 2 0.010 None 1.000 1 2002 2002
CUI: C0866588
Disease: lupus erythematodes
lupus erythematodes
disease Disease or Syndrome 6 0.010 None 1.000 1 2006 2006
CUI: C1378511
Disease: Undifferentiated leukemia
Undifferentiated leukemia
disease Neoplastic Process 120 2 0.010 None 1.000 1 2010 2010
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
disease Finding 149 527 0.100 None 1.000 1 1 2019 2019
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
phenotype Finding 147 526 0.100 None 1.000 1 1 2019 2019
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
phenotype Finding 147 526 0.100 None 1.000 1 1 2019 2019
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
phenotype Finding 147 526 0.100 None 1.000 1 1 2019 2019
CUI: C2674219
Disease: SPHEROCYTOSIS, HEREDITARY, 2
SPHEROCYTOSIS, HEREDITARY, 2
disease Disease or Syndrome 8 13 0.010 None 1.000 1 2011 2011