Google Aufzeichnung(TG:e10838).rag

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TG
- Thyroid Dyshormonogenesis 3
- Autoimmune Thyroid Disease, Susceptibility To, 3
- Thyroid Cancer, Nonmedullary, 1
- Melas Syndrome
- Thyroid Dyshormonogenesis
- Hashimoto Thyroiditis
POLG
- Myoclonic Epilepsy With Ragged Red Fibers
- Mitochondrial Myopathy
- Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive 1
- Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 1
- Melas Syndrome
- Kearns-Sayre Syndrome
- Hashimoto Thyroiditis
- Mitochondrial Dna Depletion Syndrome 1 (Mngie Type)
TRNL1
- Myoclonic Epilepsy With Ragged Red Fibers
- Mitochondrial Myopathy
- Melas Syndrome
- Kearns-Sayre Syndrome
RAG2
- Combined Immunodeficiency With Skin Granulomas
- Severe Combined Immunodeficiency Due To Complete Rag1/2 Deficiency
TRNF
- Myoclonic Epilepsy With Ragged Red Fibers
- Mitochondrial Myopathy
- Melas Syndrome
RAG1
- Combined Immunodeficiency With Skin Granulomas
- Severe Combined Immunodeficiency Due To Complete Rag1/2 Deficiency
IL1B
- Myoclonic Epilepsy With Ragged Red Fibers
- Mitochondrial Myopathy
- Thyroid Cancer, Nonmedullary, 1
- Melas Syndrome
- Kearns-Sayre Syndrome
- Hashimoto Thyroiditis
ND5
- Myoclonic Epilepsy With Ragged Red Fibers
- Mitochondrial Myopathy
- Melas Syndrome
RRM2B
- Mitochondrial Myopathy
- Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive 1
- Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 1
- Kearns-Sayre Syndrome
- Mitochondrial Dna Depletion Syndrome 1 (Mngie Type)
IL1A
- Myoclonic Epilepsy With Ragged Red Fibers
- Mitochondrial Myopathy
- Thyroid Cancer, Nonmedullary, 1
- Melas Syndrome
- Kearns-Sayre Syndrome
- Hashimoto Thyroiditis
SLC25A4
- Myoclonic Epilepsy With Ragged Red Fibers
- Mitochondrial Myopathy
- Mitochondrial Dna Depletion Syndrome 12b (Cardiomyopathic Type), Autosomal Recessive
- Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 1
- Melas Syndrome
- Kearns-Sayre Syndrome
TWNK
- Mitochondrial Myopathy
- Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 1
- Melas Syndrome
- Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 3
- Kearns-Sayre Syndrome
TRNW
- Mitochondrial Myopathy
- Melas Syndrome
TRNS1
- Myoclonic Epilepsy With Ragged Red Fibers
- Mitochondrial Myopathy
- Melas Syndrome
TRNQ
- Myoclonic Epilepsy With Ragged Red Fibers
- Mitochondrial Myopathy
- Melas Syndrome
TRNK
- Myoclonic Epilepsy With Ragged Red Fibers
- Mitochondrial Myopathy
- Melas Syndrome
CHCHD10
- Mitochondrial Myopathy
- Myopathy, Isolated Mitochondrial, Autosomal Dominant
- Frontotemporal Dementia And/or Amyotrophic Lateral Sclerosis 2
BRAF
- Thyroid Cancer, Nonmedullary, 1
- Hashimoto Thyroiditis
TRNS2
- Myoclonic Epilepsy With Ragged Red Fibers
- Mitochondrial Myopathy
- Melas Syndrome
AGK
- Mitochondrial Myopathy
- Mitochondrial Dna Depletion Syndrome 12b (Cardiomyopathic Type), Autosomal Recessive
- Thyroid Cancer, Nonmedullary, 1