TBX3, T-box transcription factor 3, 6926

N. diseases: 179; N. variants: 12
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1866994
Disease: Ulnar-mammary syndrome
Ulnar-mammary syndrome
1.000 CausalMutation disease CLINVAR
CUI: C1866994
Disease: Ulnar-mammary syndrome
Ulnar-mammary syndrome
1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.600 CausalMutation disease CGI
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.600 CausalMutation disease CGI
CUI: C0152427
Disease: Polydactyly
Polydactyly
0.300 Biomarker disease GENOMICS_ENGLAND
Neoplasm of uncertain or unknown behavior of breast
0.300 CausalMutation disease CGI
CUI: C0858252
Disease: Breast adenocarcinoma
Breast adenocarcinoma
0.300 CausalMutation disease CGI
CUI: C1867000
Disease: Hypoplastic/absent/deformed radius
Hypoplastic/absent/deformed radius
0.300 Biomarker phenotype GENOMICS_ENGLAND
CUI: C4228778
Disease: Abnormality of radial ray
Abnormality of radial ray
0.300 Biomarker phenotype GENOMICS_ENGLAND
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
0.120 Biomarker phenotype HPO
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
0.120 Biomarker group HPO
CUI: C0266013
Disease: Congenital hypoplasia of breast
Congenital hypoplasia of breast
0.110 Biomarker disease HPO
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
0.100 Biomarker disease HPO
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
0.100 Biomarker disease HPO
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.100 Biomarker disease HPO
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal
0.100 Biomarker phenotype HPO
CUI: C0020608
Disease: Hypodontia
Hypodontia
0.100 Biomarker disease HPO
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker disease HPO
CUI: C0034012
Disease: Delayed Puberty
Delayed Puberty
0.100 Biomarker phenotype HPO
CUI: C0034194
Disease: Pyloric Stenosis
Pyloric Stenosis
0.100 Biomarker phenotype HPO
CUI: C0152436
Disease: Hymen, Imperforate
Hymen, Imperforate
0.100 Biomarker disease HPO
CUI: C0152438
Disease: Sprengel deformity
Sprengel deformity
0.100 Biomarker disease HPO
CUI: C0158731
Disease: Congenital pectus carinatum
Congenital pectus carinatum
0.100 Biomarker disease HPO
CUI: C0238441
Disease: Subglottic stenosis
Subglottic stenosis
0.100 Biomarker disease HPO
CUI: C0262374
Disease: Stricture of anus
Stricture of anus
0.100 Biomarker phenotype HPO