Source: HPO

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis
0.440 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0026848
Disease: Myopathy
Myopathy
0.170 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
0.120 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly
0.110 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0240912
Disease: Vertical Talus
Vertical Talus
0.110 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly
0.110 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0006157
Disease: Breech Presentation
Breech Presentation
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0015469
Disease: Facial paralysis
Facial paralysis
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0016202
Disease: Flatfoot
Flatfoot
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0019553
Disease: Hip Contracture
Hip Contracture
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0022821
Disease: Kyphosis deformity of spine
Kyphosis deformity of spine
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0024003
Disease: Lordosis
Lordosis
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0026034
Disease: Microstomia
Microstomia
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0026267
Disease: Mitral Valve Prolapse Syndrome
Mitral Valve Prolapse Syndrome
0.100 Biomarker HPO

Entrez Id: 7169
Gene Symbol: TPM2
TPM2
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
0.100 Biomarker HPO