Pages that link to "Leigh disease"
From WikiMD's Food, Medicine & Wellness Encyclopedia
The following pages link to Leigh disease:
Displayed 40 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Pediatric glossary of terms (← links | edit)
- Pediatric glossary of terms expanded (← links | edit)
- Kearns-sayre syndrome (← links | edit)
- Pearson syndrome (← links | edit)
- Pyruvate carboxylase deficiency (← links | edit)
- Friedreich's ataxia (← links | edit)
- Mohr–Tranebjærg syndrome (← links | edit)
- Dictionary-of-medicine-L (← links | edit)
- Encyclopedia of neurology (← links | edit)
- Category:Mitochondrial diseases (← links | edit)
- List of rare diseases-L (← links | edit)
- Genetic diseases-L (← links | edit)
- Chronic progressive external ophthalmoplegia (← links | edit)
- Coenzyme Q10 deficiency (← links | edit)
- Template:Mitochondrial diseases (← links | edit)
- Diabetes and deafness (← links | edit)
- Kjer's optic neuropathy (← links | edit)
- Leber's hereditary optic neuropathy (← links | edit)
- Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes (← links | edit)
- Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis (← links | edit)
- Neuropathy ataxia retinitis pigmentosa syndrome (← links | edit)
- Myoclonic epilepsy with ragged red fibers (← links | edit)
- Mitochondrial DNA-associated Leigh syndrome (← links | edit)
- Leigh syndrome, French Canadian type (← links | edit)
- Merrf syndrome (← links | edit)
- Pearson marrow pancreas syndrome (← links | edit)
- HIBCH deficiency (← links | edit)
- MELAS syndrome (← links | edit)
- CHCHD10 (← links | edit)
- Cytochrome C oxidase deficiency (← links | edit)
- CYC1 (← links | edit)
- COX6B1 (← links | edit)
- COX7B (← links | edit)
- MT-TY (← links | edit)
- SLC25A39 (← links | edit)
- NDUFAF2 (← links | edit)
- PET100 (← links | edit)
- SCO1 (← links | edit)
- MT-TL2 (← links | edit)
- UQCC2 (← links | edit)