AR, androgen receptor, 367

N. diseases: 854; N. variants: 163
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome
1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome
1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
1.000 GeneticVariation disease UNIPROT
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
1.000 CausalMutation disease CLINVAR
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
1.000 GeneticVariation disease CLINVAR
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
1.000 Biomarker disease HPO
CUI: C0268301
Disease: Reifenstein Syndrome
Reifenstein Syndrome
0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C0268301
Disease: Reifenstein Syndrome
Reifenstein Syndrome
0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C0268301
Disease: Reifenstein Syndrome
Reifenstein Syndrome
0.800 CausalMutation disease CLINVAR
CUI: C0268301
Disease: Reifenstein Syndrome
Reifenstein Syndrome
0.800 GeneticVariation disease CLINVAR
CUI: C1839259
Disease: Bulbo-Spinal Atrophy, X-Linked
Bulbo-Spinal Atrophy, X-Linked
0.700 GermlineCausalMutation disease ORPHANET
CUI: C1839259
Disease: Bulbo-Spinal Atrophy, X-Linked
Bulbo-Spinal Atrophy, X-Linked
0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C1839259
Disease: Bulbo-Spinal Atrophy, X-Linked
Bulbo-Spinal Atrophy, X-Linked
0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.600 GeneticVariation disease UNIPROT
CUI: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate
0.600 CausalMutation disease CGI
CUI: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate
0.600 GenomicAlterations disease CGI
CUI: C2678098
Disease: Hypospadias 1, X-Linked
Hypospadias 1, X-Linked
0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C2678098
Disease: Hypospadias 1, X-Linked
Hypospadias 1, X-Linked
0.600 CausalMutation disease CLINVAR
CUI: C2678098
Disease: Hypospadias 1, X-Linked
Hypospadias 1, X-Linked
0.600 Biomarker disease CTD_human
CUI: C2678098
Disease: Hypospadias 1, X-Linked
Hypospadias 1, X-Linked
0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.390 Biomarker disease HPO
Diabetes Mellitus, Non-Insulin-Dependent
0.370 Biomarker disease HPO
Diabetes Mellitus, Non-Insulin-Dependent
0.370 Biomarker disease MGD
CUI: C0393547
Disease: Bulbospinal Neuronopathy
Bulbospinal Neuronopathy
0.360 GermlineCausalMutation disease ORPHANET