MT-TV - mitochondrially encoded tRNA valine Gene

Also Known as MTTV; TRNV

Species: Homo sapiens

Gene Type: tRNA
Gene ID: 4577

Related Diseases

Diseases Alias
Charcot-Marie-Tooth Disease, Axonal, Mitochondrial Form, 1

  • CMTMA1
Mitochondrial Dna-Associated Leigh Syndrome

  • Mils

  • Maternally Inherited Leigh Syndrome

  • Leigh Disease, Maternally Inherited

  • Subacute Necrotizing Encephalomyelopathy Maternally Inherited

  • Maternally-Inherited Leigh Disease

  • Maternally-Inherited Infantile Subacute Necrotizing Encephalopathy

  • Mtdna-Associated Leigh Syndrome
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes

  • Melas Syndrome

  • MELAS

  • Mitochondrial Encephalomyopathy Lactic Acidosis And Stroke-Like Episodes

  • Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode

  • Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes

  • Myopathy, Mitochondrial-Encephalopathy-Lactic Acidosis-Stroke

  • Mitochondrial Encephalomyopathy, Lactic Acidosis And Stroke-Like Episodes

  • Mitochondrial Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes

  • Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis And Stroke-Like Episodes

  • Mitochondrial Encephalomyopathy With Lactic Acidosis And Stroke-Like Episodes Syndrome

  • Myopathy, Mitochondrial, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes
Leigh Syndrome

  • Leigh Disease

  • Infantile Subacute Necrotizing Encephalopathy

  • Leigh Syndrome Due To Mitochondrial Complex Iv Deficiency

  • LS

  • Sne

  • Leigh'S Disease

  • Leigh Syndrome Due To Mitochondrial Complex I Deficiency

  • Necrotizing Encephalopathy, Infantile Subacute, Of Leigh

  • Subacute Necrotizing Encephalomyelopathy

  • Necrotizing Encephalopathy Infantile Subacute Of Leigh

  • Leigh Syndrome Due To Mitochondrial Complex Iii Deficiency

  • Infantile Necrotizing Encephalomyelopathy

  • Juvenile Subacute Necrotizing Encephalomyelopathy

  • Leigh'S Necrotizing Encephalopathy

  • Subacute Necrotizing Encephalopathy

  • Juvenile Subacute Necrotizing Encephalopathy

  • Leigh Syndrome Due To Mitochondrial Complex Ii Deficiency

  • Leigh Syndrome Due To Mitochondrial Complex V Deficiency

  • Encephalopathy, Subacute Necrotizing, Infantile

  • Encephalopathy, Subacute Necrotizing, Juvenile

  • Maternally Inherited Leigh Syndrome

  • Subacute Necrotising Encephalomyelopathy

  • Subacute Necrotising Encephalopathy
Retinitis Pigmentosa 36

  • RP36

  • Retinitis Pigmentosa-36

  • Retinitis Pigmentosa, Type 36
Mitochondrial Disease

  • Mitochondrial Diseases

  • Mitochondrial Disorder
Retinitis Pigmentosa 20

  • RP20

  • Retinitis Pigmentosa, Type 20
Carbuncle

  • Carbuncle And Furuncle Of Any Part Of Face Except Eye

  • Carbuncle And Furuncle Of Buttock

  • Carbuncle And Furuncle Of Face

  • Carbuncle And Furuncle Of Foot

  • Carbuncle And Furuncle Of Gluteal Region

  • Carbuncle And Furuncle Of Hand

  • Carbuncle And Furuncle Of Leg Except Foot

  • Carbuncle And Furuncle Of Neck

  • Carbuncle And Furuncle Of Trunk

  • Carbuncle And Furuncle Of Upper Arm And Forearm
Retinitis Pigmentosa 14

  • RP14

  • Retinitis Pigmentosa Juvenile Tulp1-Related

  • Retinitis Pigmentosa-14

  • Retinitis Pigmentosa, Type 14
Intellectual Developmental Disorder, Autosomal Dominant 30, With Speech Delay And Behavioral Abnormalities

  • MRD30

  • Mental Retardation, Autosomal Dominant 30

  • Intellectual Developmental Disorder, Autosomal Dominant 30

  • Autosomal Dominant Non-Syndromic Intellectual Disability 30

  • Autosomal Dominant Intellectual Developmental Disorder 30

  • Autosomal Dominant Mental Retardation 30

  • Mental Retardation, Autosomal Dominant, Type 30
Mitochondrial Dna Depletion Syndrome 4b

  • Mitochondrial Neurogastrointestinal Encephalopathy Syndrome

  • Mngie Syndrome

  • Thymidine Phosphorylase Deficiency

  • MTDPS4B

  • Mitochondrial Neurogastrointestinal Encephalopathy Disease

  • Mngie

  • Myoneurogastrointestinal Encephalopathy Syndrome

  • Ogimd

  • Oculogastrointestinal Muscular Dystrophy

  • Polip

  • Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, And Intestinal Pseudo-Obstruction

  • Mitochondrial Neurogastrointestinal Encephalopathy Syndrome, Polg-Related

  • Mngie, Polg-Related

  • Mepop

  • Mitochondrial Myopathy With Sensorimotor Polyneuropathy, Ophthalmoplegia, And Pseudo-Obstruction

  • Mngie Disease

  • Mitochondrial Dna Depletion Syndrome 4b Mngie Type

  • Mitochondrial Neurogastrointestinal Encephalopathy Syndrome Polg-Related

  • Mngie Polg-Related

  • Mitochondrial Dna Depletion Syndrome, Type 4b

  • Visceral Myopathy Familial External Ophthalmoplegia
Leber Hereditary Optic Neuropathy, Modifier Of

  • Leber Optic Atrophy

  • Leber Hereditary Optic Neuropathy

  • LHON

  • Leber'S Hereditary Optic Neuropathy

  • Leber Optic Atrophy, Susceptibility To

  • Leber'S Optic Atrophy

  • LOAM

  • Loas

  • Leber'S Disease

  • Leber'S Optic Neuropathy

  • Optic Atrophy, Hereditary, Leber

  • Lhon, Modifier Of

  • Optic Atrophy, Leber Type

  • Hereditary Optic Neuroretinopathy

  • Leber Hereditary Optic Atrophy

  • Loa

  • Optic Atrophy Leber Type

  • Leber Hereditary Optic Neuropathy, Modifier

  • Leber Hereditary Optic Neuropathy Susceptibility

  • Modifier Of Leber Hereditary Optic Neuropathy

  • Lebers Hereditary Optic Neuropathy

  • Leber Congenital Amaurosis
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma