MT-TD - mitochondrially encoded tRNA aspartic acid Gene

Also Known as MTTD; TRND

Species: Homo sapiens

Gene Type: tRNA
Gene ID: 4555

Related Diseases

Diseases Alias
Mitochondrial Disease

  • Mitochondrial Diseases

  • Mitochondrial Disorder
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
Noonan Syndrome 13

  • NS13
Myasthenic Syndrome, Congenital, 4c, Associated With Acetylcholine Receptor Deficiency

  • Congenital Myasthenic Syndrome 4c

  • CMS4C

  • Cms Id

  • Cms1d

  • Congenital Myasthenic Syndrome Type Id

  • Fim1

  • Myasthenic Syndrome, Congenital, Associated With Acetylcholine Receptor Deficiency

  • Myasthenic Syndrome, Congenital, Type Id

  • Cms1d, Formerly

  • Cms Id, Formerly

  • Myasthenia, Familial Infantile, 1, Formerly

  • Fim1, Formerly

  • Congenital Myasthenic Syndrome 4c Associated With Acetylcholine Receptor Deficiency

  • Familial Infantile Myasthenia 1

  • Cms1e

  • Cms-Achrd

  • Cms Ie

  • Congenital Myasthenic Syndrome Post-Synaptic Associated With Acetylcholine Receptor Deficiency

  • Congenital Myasthenic Syndrome Type 1d

  • Congenital Myasthenic Syndrome Type 1e

  • Congenital Myasthenic Syndrome Type Ie

  • Congenital Myasthenic Syndrome With Facial Dysmorphism Associated With Acetylcholine Receptor Deficiency

  • Myasthenia, Familial Infantile, 1

  • Myasthenic Syndrome, Congenital, Type 4c, Associated With Acetylcholine Receptor Deficiency

  • Myasthenic Syndrome, Congenital, Ie
Trench Fever

  • His-Werner Disease

  • Quintan Fever

  • Shin Bone Fever

  • Wolhynian Fever

  • Tibialgic Fever

  • Bartonellosis Due To Bartonella Quintana Infection

  • Febris Quintata

  • Five Day Fever

  • Fever Due To Rickettsia Quintana

  • Febris Quintana

  • Fever Due To Bartonella Quintana

  • Fever Due To Rochalimaea Quintana

  • Meuse Fever
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