Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.490 Biomarker disease CTD_human
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.490 Biomarker disease HPO
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
0.350 FusionGene disease ORPHANET
CUI: C0026998
Disease: Acute Myeloid Leukemia, M1
Acute Myeloid Leukemia, M1
0.300 Biomarker disease CTD_human
CUI: C1879321
Disease: Acute Myeloid Leukemia (AML-M2)
Acute Myeloid Leukemia (AML-M2)
0.300 Biomarker disease CTD_human
CUI: C0544886
Disease: Somatic mutation
Somatic mutation
0.100 Biomarker phenotype HPO
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.500 GeneticVariation disease BEFREE <b>Background:</b> Phosphatidylinositol binding clathrin assembly protein (<i>PICALM</i>) rs541458 C allele has been identified and validated to be associated with a reduction of Alzheimer's disease (AD) risk. 31133980 2019
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.500 GeneticVariation disease BEFREE (2) Four additional AD risk SNPs were nominally associated with obesity (rs17125944 at FERMT2, pBMI  = 4.03 × 10(-05), pBMI corr  = 2.50 × 10(-03) ; rs3851179 at PICALM; pBMI  = 0.002, rs2075650 at TOMM40/APOE, pBMI  = 0.024, rs3865444 at CD33, pBMI  = 0.024). 24788522 2014
CUI: C0028754
Disease: Obesity
Obesity
0.010 GeneticVariation disease BEFREE (2) Four additional AD risk SNPs were nominally associated with obesity (rs17125944 at FERMT2, pBMI  = 4.03 × 10(-05), pBMI corr  = 2.50 × 10(-03) ; rs3851179 at PICALM; pBMI  = 0.002, rs2075650 at TOMM40/APOE, pBMI  = 0.024, rs3865444 at CD33, pBMI  = 0.024). 24788522 2014
CUI: C0268398
Disease: Familial lichen amyloidosis
Familial lichen amyloidosis
0.010 GeneticVariation disease BEFREE 63) associated nominally significantly with posterior AD, and rs3851179 at the PICALM locus had significant association with PCA (p = 0.0003, OR = 2.84). 24670887 2014
CUI: C3888194
Disease: MIXED LINEAGE LEUKEMIA
MIXED LINEAGE LEUKEMIA
0.030 GeneticVariation disease BEFREE Mixed-lineage leukemia with t(10;11)(p13;q21): an analysis of AF10-CALM and CALM-AF10 fusion mRNAs and clinical features. 10221337 1999
M5b Acute differentiated monocytic leukemia
0.010 GeneticVariation disease BEFREE Monocytic leukemia with CALM/AF10 rearrangement showing mediastinal emphysema. 12555219 2003
CUI: C0598894
Disease: Monocytic leukemia
Monocytic leukemia
0.010 GeneticVariation disease BEFREE Monocytic leukemias with CALM/AF10 fusion are frequently associated with mediastinal invasion. 12555219 2003
CUI: C0023418
Disease: leukemia
leukemia
0.100 Biomarker disease BEFREE CALM-AF10 fusion gene in leukemias: simple and inversion-associated translocation (10;11). 11106826 2000
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.070 Biomarker disease BEFREE CALM-AF10 mice infected with the MOL4070LTR retrovirus developed acute leukemia, and ligation-mediated polymerase chain reaction was used to identify retroviral insertions at 19 common insertion sites, including Zeb2, Nf1, Mn1, Evi1, Ift57, Mpl, Plag1, Kras, Erg, Vav1, and Gata1. 20007546 2010
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.500 GeneticVariation disease BEFREE PICALM, the gene encoding phosphatidylinositol-binding clathrin assembly (picalm) protein, was recently shown to be associated with risk of Alzheimer disease (AD). 20838239 2010
CUI: C1843013
Disease: Alzheimer disease, familial, type 3
Alzheimer disease, familial, type 3
0.010 Biomarker disease BEFREE PICALM might play an important role in AD pathology through participating in altering synaptic vesicle cycling or APP endocytosis. 20951388 2011
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.500 GeneticVariation disease BEFREE PICALM and CR1 variants are not associated with sporadic Alzheimer's disease in Chinese patients. 21358043 2011
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.360 Biomarker disease BEFREE PICALM was associated with an earlier age at midpoint of cognitive decline. 22952074 2012
CUI: C0234985
Disease: Mental deterioration
Mental deterioration
0.330 Biomarker phenotype BEFREE PICALM was associated with an earlier age at midpoint of cognitive decline. 22952074 2012
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.500 GeneticVariation disease BEFREE PICALM gene rs3851179 polymorphism contributes to Alzheimer's disease in an Asian population. 23572399 2013
Precursor Cell Lymphoblastic Leukemia Lymphoma
0.040 Biomarker disease BEFREE CALM-AF10 fusion within early T-cell precursor acute lymphoblastic leukemia (21%) did, however, identify a group with a poor prognosis with regards to event-free survival (P=0.04). 23831922 2013
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
0.350 Biomarker disease BEFREE CALM-AF10 therefore identifies a poor prognostic group within sCD3/T-cell receptor negative adult T-cell acute lymphoblastic leukemias and is over-represented within early T-cell precursor acute lymphoblastic leukemias, in which it identifies patients in whom treatment is likely to fail. 23831922 2013
Adult T Acute Lymphoblastic Leukemia
0.010 Biomarker disease BEFREE CALM-AF10 therefore identifies a poor prognostic group within sCD3/T-cell receptor negative adult T-cell acute lymphoblastic leukemias and is over-represented within early T-cell precursor acute lymphoblastic leukemias, in which it identifies patients in whom treatment is likely to fail. 23831922 2013
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.060 Biomarker disease BEFREE CALM-AF10 therefore identifies a poor prognostic group within sCD3/T-cell receptor negative adult T-cell acute lymphoblastic leukemias and is over-represented within early T-cell precursor acute lymphoblastic leukemias, in which it identifies patients in whom treatment is likely to fail. 23831922 2013