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Diseases
Genes (534)
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TRNL1
Merrf Syndrome
Melas
Maternally Inherited Diabetes And Deafness
TRNF
Merrf Syndrome
Melas
TRNS1
Merrf Syndrome
Melas
Palmoplantar Keratoderma With Deafness
ND5
Merrf Syndrome
Melas
Maternally Inherited Diabetes And Deafness
TRNK
Merrf Syndrome
Melas
Maternally Inherited Diabetes And Deafness
ABHD5
Cerebral Creatine Deficiency
ND1
Melas
Mitochondrial Complex I Deficiency
ELAC2
Combined Oxidative Phosphorylation Deficiency 17
Mitochondrial Complex I Deficiency
MLH1
Muir–torre Syndrome
Deafness-Dystonia-Optic Neuronopathy Syndrome
Gastric Lymphoma
MSH2
Muir–torre Syndrome
Deafness-Dystonia-Optic Neuronopathy Syndrome
GAMT
Guanidinoacetate Methyltransferase Deficiency
TRNQ
Merrf Syndrome
Melas
NDUFS4
Mitochondrial Complex I Deficiency
PRG4
Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome
TRNS2
Merrf Syndrome
Melas
TIMM8A
Deafness-Dystonia-Optic Neuronopathy Syndrome
RHBDF2
Howel–evans Syndrome
TRNP
Merrf Syndrome
Melas
DYNC2H1
Short-Rib Thoracic Dysplasia 11 With Or Without Polydactyly
TRNH
Merrf Syndrome
Melas