Source: ALL

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: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C4721453
Disease: Peripheral Nervous System Diseases
Peripheral Nervous System Diseases 		group 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1806780
Disease: Increased CSF protein
Increased CSF protein 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0852413
Disease: Abnormal muscle tone
Abnormal muscle tone 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0563243
Disease: Poor coordination
Poor coordination 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures 		disease 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0036572
Disease: Seizures
Seizures 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases 		group 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1833431
Disease: Subependymal cysts
Subependymal cysts 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1836923
Disease: Gastrointestinal dysmotility
Gastrointestinal dysmotility 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C4280681
Disease: Gastrojejunal tube feeding in infancy
Gastrojejunal tube feeding in infancy 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C4021758
Disease: Delayed CNS myelination
Delayed CNS myelination 		disease 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C3806442
Disease: Myoclonic spasms
Myoclonic spasms 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C3149083
Disease: Decreased activity of mitochondrial complex III
Decreased activity of mitochondrial complex III 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C2677180
Disease: Congenital microcephaly
Congenital microcephaly 		disease 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1962966
Disease: Retinopathy, CTCAE
Retinopathy, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1854699
Disease: Diffuse cerebellar atrophy
Diffuse cerebellar atrophy 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1837496
Disease: Axonal degeneration
Axonal degeneration 		phenotype 0.100 None 0 0