IGF2, insulin like growth factor 2, 3481

N. diseases: 604; N. variants: 19
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.900 Biomarker phenotype HPO
CUI: C0175693
Disease: Russell-Silver syndrome
Russell-Silver syndrome
0.700 CausalMutation disease CLINVAR
CUI: C0206624
Disease: Hepatoblastoma
Hepatoblastoma
0.700 Biomarker disease HPO
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 Biomarker disease HPO
CUI: C0004903
Disease: Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome
0.600 Biomarker disease GENOMICS_ENGLAND
GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES
0.600 CausalMutation disease CLINVAR
GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES
0.600 Biomarker disease CTD_human
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma
0.500 Biomarker disease HPO
CUI: C0206686
Disease: Adrenocortical carcinoma
Adrenocortical carcinoma
0.500 Biomarker disease HPO
CUI: C0271708
Disease: Fasting Hypoglycemia
Fasting Hypoglycemia
0.410 Biomarker phenotype HPO
CUI: C0332890
Disease: Congenital hemihypertrophy
Congenital hemihypertrophy
0.400 Biomarker disease HPO
Diabetes Mellitus, Insulin-Dependent
0.300 Biomarker disease MGD
DIABETES MELLITUS, INSULIN-DEPENDENT, 2
0.200 Biomarker disease MGD
CUI: C3837958
Disease: Diabetes Mellitus, Ketosis-Prone
Diabetes Mellitus, Ketosis-Prone
0.200 Biomarker disease MGD
diabetes (mellitus) due to autoimmune process
0.200 Biomarker disease MGD
diabetes (mellitus) due to immune mediated pancreatic islet beta-cell destruction
0.200 Biomarker disease MGD
CUI: C4290092
Disease: idiopathic diabetes (mellitus)
idiopathic diabetes (mellitus)
0.200 Biomarker disease MGD
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.130 Biomarker disease HPO
CUI: C0036631
Disease: Seminoma
Seminoma
0.110 Biomarker disease HPO
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers
0.110 Biomarker disease HPO
CUI: C0271561
Disease: Somatotropin deficiency
Somatotropin deficiency
0.110 Biomarker disease HPO
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
0.110 Biomarker disease HPO
CUI: C1849075
Disease: Relative macrocephaly
Relative macrocephaly
0.110 Biomarker disease HPO
CUI: C0010276
Disease: Craniopharyngioma
Craniopharyngioma
0.100 Biomarker disease HPO
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
0.100 Biomarker disease HPO