SETBP1, SET binding protein 1, 26040

N. diseases: 257; N. variants: 28
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0265227
Disease: Schinzel-Giedion syndrome
Schinzel-Giedion syndrome
0.770 GeneticVariation disease CLINVAR
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.590 CausalMutation disease CGI
Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative
0.590 CausalMutation disease CGI
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME
0.570 CausalMutation group CGI
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
0.500 CausalMutation disease CGI
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
0.410 Biomarker group HPO
CUI: C0023470
Disease: Myeloid Leukemia
Myeloid Leukemia
0.400 Biomarker disease HPO
MENTAL RETARDATION, AUTOSOMAL DOMINANT 29
0.400 Biomarker disease CTD_human
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.310 GeneticVariation disease UNIPROT
CUI: C0027019
Disease: Myelomonocytic leukemia
Myelomonocytic leukemia
0.300 CausalMutation disease CGI
Dysembryoplastic neuroepithelial tumor
0.300 CausalMutation disease CGI
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy
0.110 GeneticVariation disease CLINVAR
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy
0.110 Biomarker disease HPO
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
0.100 Biomarker disease HPO
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
0.100 Biomarker disease HPO
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0.100 Biomarker group HPO
CUI: C0014474
Disease: Ependymoma
Ependymoma
0.100 Biomarker disease HPO
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
0.100 Biomarker disease HPO
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
0.100 Biomarker group HPO
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
0.100 Biomarker group HPO
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
0.100 GeneticVariation group CLINVAR
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal
0.100 Biomarker phenotype HPO
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease
0.100 Biomarker disease HPO
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis
0.100 Biomarker disease HPO
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis
0.100 GeneticVariation disease CLINVAR