MT-TH - mitochondrially encoded tRNA histidine Gene

Also Known as MTTH; TRNH

Species: Homo sapiens

Gene Type: tRNA
Gene ID: 4564

Related Diseases

Diseases Alias
Mitochondrial Disease With Hypertrophic Cardiomyopathy
  • Cardiomyopathy, Hypertrophic, Mitochondrial

Deafness, Nonsyndromic Sensorineural, Mitochondrial
  • Mitochondrial Non-Syndromic Sensorineural Hearing Loss

  • Mitochondrial Nonsyndromic Sensorineural Deafness

  • Mitochondrial Non-Syndromic Sensorineural Deafness

  • Isolated Mitochondrial Neurosensory Deafness

  • Isolated Mitochondrial Neurosensory Hearing Loss

  • Isolated Mitochondrial Sensorineural Deafness

  • Isolated Mitochondrial Sensorineural Hearing Loss

  • Mitochondrial Non-Syndromic Neurosensory Deafness

  • Mitochondrial Non-Syndromic Neurosensory Hearing Loss

  • Deafness, Sensorineural, Mitochondrial

  • DFNM

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

Myoclonic Epilepsy Associated With Ragged-Red Fibers
  • Merrf Syndrome

  • MERRF

  • Fukuhara Syndrome

  • Myoclonic Epilepsy Associated With Ragged Red Fibers

  • Myoencephalopathy Ragged-Red Fiber Disease

  • Myoclonic Epilepsy - Ragged Red Fibers

  • Myoclonus Epilepsy And Ragged Red Fibers

  • Myoclonus With Epilepsy And With Ragged Red Fibers

  • Myoclonic Epilepsy With Ragged Red Fibers

  • Myoclonic Epilepsy With Ragged-Red Fibers

  • Fukuhara Disease

  • Myoclonus Epilepsy Associated With Ragged-Red Fibres

  • Myoclonus With Epilepsy With Ragged Red Fibers

Mitochondrial Disease
  • Mitochondrial Diseases

  • Mitochondrial Disorder

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

Hermaphroditism
Retinitis Pigmentosa 36
  • RP36

  • Retinitis Pigmentosa-36

  • Retinitis Pigmentosa, Type 36

Bjornstad Syndrome
  • BJS

  • Pili Torti And Nerve Deafness

  • Ptd

  • Pili Torti-Deafness Syndrome

  • Deafness-Pili Torti-Hypogonadism Syndrome

  • Deafness And Pili Torti, Bjornstad Type

  • Pili Torti-Sensorineural Hearing Loss

  • Björnstad Syndrome

  • Ptnd

  • Hearing Loss-Pili Torti-Hypogonadism Syndrome

  • Bjoernstad Syndrome

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

Hemorrhoid
  • Hemorrhoids

  • Hemorrhoidal Disease

  • Rectal Diseases

  • Piles

  • Unspecified Haemorrhoids Without Complication

Dysentery
  • Infectious Diarrhea

Autoimmune Lymphoproliferative Syndrome
  • ALPS

  • Canale-Smith Syndrome

  • Autoimmune Lymphoproliferative Syndrome, Type Ia

  • Autoimmune Lymphoproliferative Syndrome, Type Ib

  • Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant

  • Css

  • Autoimmune Lymphoproliferative Syndrome, Type 1b

  • Autoimmune Lymphoproliferative Syndrome, Type 1a

  • Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant

  • Fas Deficiency

  • Autoimmune Lymphoproliferative Syndrome 1a

  • ALPS1A

  • Autoimmune Lymphoproliferative Syndrome Type Ia

  • Autoimmune Lymphoproliferative Syndrome 1b

  • ALPS1B

  • Autoimmune Lymphoproliferative Syndrome Type Ib

Stuttering
  • Stammering

  • Familial Persistent Stuttering

  • Stuttering, Familial Persistent 1

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