Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0162674
Disease: Chronic progressive external ophthalmoplegia
Chronic progressive external ophthalmoplegia 		0.400 GermlineCausalMutation ORPHANET Pathogenic mitochondrial tRNA point mutations: nine novel mutations affirm their importance as a cause of mitochondrial disease. 23696415

2013
Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0162674
Disease: Chronic progressive external ophthalmoplegia
Chronic progressive external ophthalmoplegia 		0.400 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0268237
Disease: Cytochrome-c Oxidase Deficiency
Cytochrome-c Oxidase Deficiency 		0.400 Biomarker CTD_human

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0268237
Disease: Cytochrome-c Oxidase Deficiency
Cytochrome-c Oxidase Deficiency 		0.400 CausalMutation CLINVAR

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0002871
Disease: Anemia
Anemia 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0004134
Disease: Ataxia
Ataxia 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0017979
Disease: Glycosuria
Glycosuria 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0033377
Disease: Ptosis
Ptosis 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0033687
Disease: Proteinuria
Proteinuria 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0036572
Disease: Seizures
Seizures 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0151747
Disease: Renal tubular disorder
Renal tubular disorder 		0.100 Biomarker HPO

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0162292
Disease: External Ophthalmoplegia
External Ophthalmoplegia 		0.100 CausalMutation CLINVAR

Entrez Id: 4570
Gene Symbol: TRNN
TRNN
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome 		0.100 CausalMutation CLINVAR