Source: INFERRED

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: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome 		disease 0.400 None 1.000 7 2 1998 2015
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		disease 0.100 None 1.000 2 2 1997 2002
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		phenotype 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C1836830
Disease: Developmental regression
Developmental regression 		disease 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		phenotype 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting 		phenotype 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C1839532
Disease: Low plasma citrulline
Low plasma citrulline 		phenotype 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C1842820
Disease: Cardiac conduction abnormality
Cardiac conduction abnormality 		phenotype 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C1843077
Disease: Segmental peripheral demyelination/remyelination
Segmental peripheral demyelination/remyelination 		phenotype 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		phenotype 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		disease 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		phenotype 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis 		phenotype 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C0497327
Disease: Dementia
Dementia 		disease 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures 		disease 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C0452138
Disease: Sensorineural hearing loss, bilateral
Sensorineural hearing loss, bilateral 		disease 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C0410916
Disease: Neonatal Death
Neonatal Death 		phenotype 0.100 None 0 1
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy 		disease 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C1843156
Disease: Progressive sensorineural hearing impairment
Progressive sensorineural hearing impairment 		disease 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		phenotype 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C1844945
Disease: Episodic respiratory distress
Episodic respiratory distress 		phenotype 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		disease 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C4531122
Disease: Abnormal speech prosody
Abnormal speech prosody 		phenotype 0.100 None 0 0
Entrez Id: 4577
Gene Symbol: TRNV
TRNV 		tRNA 0.670 0.423
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		phenotype 0.100 None 0 0