Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C1839463
Disease: TARP syndrome
TARP syndrome 		0.770 Biomarker CTD_human

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		0.410 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.300 GeneticVariation UNIPROT

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.120 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0265931
Disease: Persistent left superior vena cava
Persistent left superior vena cava 		0.110 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0003578
Disease: Apnea
Apnea 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0010520
Disease: Cyanosis
Cyanosis 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0018952
Disease: Extramedullary Hematopoiesis Function
Extramedullary Hematopoiesis Function 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0025990
Disease: Micrognathism
Micrognathism 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0027092
Disease: Myopia
Myopia 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0031900
Disease: Pierre Robin Syndrome
Pierre Robin Syndrome 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0036572
Disease: Seizures
Seizures 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0158733
Disease: Hand polydactyly
Hand polydactyly 		0.100 Biomarker HPO

Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL 		0.100 Biomarker HPO