MT-TR - mitochondrially encoded tRNA arginine Gene

Also Known as MTTR; TRNR

Species: Homo sapiens

Gene Type: tRNA
Gene ID: 4573

Related Diseases

Diseases Alias
Mitochondrial Encephalomyopathy

  • Mitochondrial Encephalomyopathies

  • Encephalomyopathy, Mitochondrial
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
Wild-Type Amyloidosis

  • Senile Systemic Amyloidosis

  • Attrwt Amyloidosis

  • Age Related Amyloidosis

  • Old Age Amyloidosis

  • Wild-Type Attr Amyloidosis

  • Wild-Type Transthyretin Cardiac Amyloidosis

  • Wild Type Attr Amyloidosis

  • Attrwt-Related Amyloidosis

  • Wild Type Attr-Related Amyloidosis
Amyloidosis, Hereditary, Transthyretin-Related

  • Transthyretin Amyloidosis

  • Familial Amyloid Polyneuropathy

  • Ttr Amyloid Neuropathy

  • Transthyretin Amyloid Neuropathy

  • Transthyretin Amyloid Polyneuropathy

  • Fap

  • Familial Transthyretin Amyloidosis

  • Amyloidosis Transthyretin Related

  • Type I Familial Amyloid Polyneuropathy

  • Familial Amyloid Polyneuropathy Type I

  • Attrv122i Amyloidosis

  • Hereditary Amyloidosis, Transthyretin-Related

  • Amyloid Polyneuropathy, Familial

  • Attr Amyloidosis

  • Attrm Amyloidosis

  • Corino De Andrade'S Disease

  • Paramyloidosis

  • Transthyretin-Related Hereditary Amyloidosis

  • Ttr Amyloidosis

  • Hereditary Attr Amyloidosis

  • Portuguese Polyneuritic Amyloidosis

  • Portuguese Type Familial Amyloid Neuropathy

  • Swiss Type Amyloid Polyneuropathy

  • Type Ii Familial Amyloid Polyneuropathy

  • Attrv30m Amyloidosis

  • Attrv30m-Related Amyloidosis

  • Familial Amyloid Polyneuropathy, Portuguese-Swedish-Japanese Type

  • Attr Cardiomyopathy

  • Attrv122i-Related Amyloidosis

  • Ttr-Related Amyloid Cardiomyopathy

  • Ttr-Related Cardiac Amyloidosis

  • Transthyretin Amyloid Cardiopathy

  • Transthyretin-Related Familial Amyloid Cardiomyopathy

  • Amyloidosis, Transthyretin-Related

  • AMYL-TTR

  • Amyloidosis I

  • Amyloidosis Ohio Type

  • Amyloidosis Type 7

  • Amyloidosis Vii

  • Amyloid Polyneuropathy

  • Attr

  • Familial Amyloid Polyneuropathy Type Ii

  • Hereditary Amyloidosis Transthyretin-Related

  • Leptomeningeal Amyloidosis

  • Meningocerebrovascular Amyloidosis

  • Oculoleptomeningeal Amyloidosis

  • Familial Amyloid Polyneuropathies

  • Amyloidosis, Leptomeningeal

  • Senile Cardiac Amyloidosis

  • Amyloid Neuropathies, Familial

  • Danish Type Familial Amyloid Cardiomyopathy

  • Familial Amyloid Neuropathy, Portuguese Type

  • Amyloid Polyneuropathy, Swiss Type

  • Hereditary Oculoleptomeningeal Amyloid Angiopathy

  • Amyloid Neuropathies
Autonomic Peripheral Neuropathy

  • Peripheral Autonomic Nervous System Diseases
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
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

Related Agents

  • Approval
  • Pre-clinical Phase

Approval

Bioactive Molecules (3)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-14852 Tafamidis Inhibitor 99.93% Yes
HY-14852A Tafamidis meglumine 99.79% Yes
HY-14852R Tafamidis (Standard) Inhibitor 99.24% Unkown

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-14852S Tafamidis-d3 / Unkown