The following pages link to Exercise intolerance
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Allergic bronchopulmonary aspergillosis (links | edit)
- Da Costa's syndrome (links | edit)
- Muscle atrophy (links | edit)
- Contracture (links | edit)
- Amyotrophy (links | edit)
- Diastasis (pathology) (links | edit)
- Bethlem myopathy (links | edit)
- Diastasis recti (links | edit)
- Second wind (links | edit)
- Vitamin B12 deficiency (links | edit)
- Anterior compartment syndrome (links | edit)
- MT-TL1 (links | edit)
- Cytochrome c oxidase subunit I (links | edit)
- Cytochrome c oxidase subunit 2 (links | edit)
- Cytochrome c oxidase subunit III (links | edit)
- MT-CYB (links | edit)
- SURF1 (links | edit)
- SCO1 (links | edit)
- NDUFS8 (links | edit)
- BCS1L (links | edit)
- COX6B1 (links | edit)
- Broxyquinoline (links | edit)
- UQCRB (links | edit)
- UQCRC2 (links | edit)
- Monocarboxylate transporter 1 (links | edit)
- ISCU (links | edit)
- Inborn errors of carbohydrate metabolism (links | edit)
- Muscle contracture (links | edit)
- Metabolic myopathy (links | edit)
- Atrial fibrillation (links | edit)
- MT-TD (links | edit)
- MT-TP (links | edit)
- MT-TY (links | edit)
- Dopamine beta hydroxylase deficiency (links | edit)
- Review of systems (links | edit)
- Ullrich congenital muscular dystrophy (links | edit)
- Hoffmann syndrome (links | edit)
- Cramp fasciculation syndrome (links | edit)
- Purine nucleotide cycle (links | edit)
- Omecamtiv mecarbil (links | edit)
- Tremovirus (links | edit)
- Myopathy, X-linked, with excessive autophagy (links | edit)
- ACO2 (links | edit)
- PGAM2 (links | edit)
- CHCHD10 (links | edit)
- TTC19 (links | edit)
- LYRM7 (links | edit)
- COA3 (links | edit)
- COA5 (links | edit)
- COX14 (links | edit)