Source: HPO

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C0518656
Disease: Chronic fatigue
Chronic fatigue
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C1836003
Disease: Facial diplegia
Facial diplegia
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
Progressive proximal muscle weakness
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C1836830
Disease: Developmental regression
Developmental regression
disease 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay
disease 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C1842587
Disease: Sensory axonal neuropathy
Sensory axonal neuropathy
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
Intellectual disability, progressive
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
Parkinsonism with favorable response to dopaminergic medication
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
Loss of ability to walk in early childhood
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy
disease 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay
disease 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C0587246
Disease: Muscle weakness of limb
Muscle weakness of limb
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C0694550
Disease: Recurrent pneumonia
Recurrent pneumonia
disease 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
disease 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C0858618
Disease: Dyschromatopsia
Dyschromatopsia
disease 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
group 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C0948163
Disease: Leukoaraiosis
Leukoaraiosis
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C1854301
Disease: Motor delay
Motor delay
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
CUI: C1856408
Disease: Infantile encephalopathy
Infantile encephalopathy
phenotype 0.100 None 0 0
Entrez Id: 7084
Gene Symbol: TK2
TK2
thymidine kinase 2 0.585 0.615 3.9E-07
Infantile sensorineural hearing impairment
phenotype 0.100 None 0 0