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Showing below up to 50 results in range #26,701 to #26,750.
- Ketoacidosis due to beta-ketothiolase deficiency (Q86109)
- Sporadic Juvenile-onset primary dystonia (Q86108)
- Acquisition of necessities (Q86107)
- Complete agenesis of pericardium (Q86106)
- Trichostrongyliasis due to Trichostrongylus orientalis (Q86105)
- Household tasks (Q86104)
- Trichostrongyliasis due to Trichostrongylus colubriformis (Q86103)
- Trichostrongyliasis due to Trichostrongylus axei (Q86102)
- Truncal dystonia (Q86101)
- Pleuropericardial cyst (Q86100)
- Chronic obstructive pulmonary disease with acute exacerbation, unspecified, moderate airflow limitation (Q86099)
- Chronic obstructive pulmonary disease with acute exacerbation, unspecified, severe airflow limitation (Q86098)
- Caring for household objects and assisting others (Q86097)
- Congenital tumour of the serous pericardium (Q86096)
- Chronic obstructive pulmonary disease with acute exacerbation, unspecified, very severe airflow limitation (Q86095)
- Partial agenesis of pericardium (Q86094)
- Adult-onset sporadic primary dystonia (Q86093)
- Parietal lobe abscess (Q86092)
- Pedal cyclist injured in collision with railway train or railway vehicle (Q86091)
- Lipoma of appendix (Q86090)
- Primary dystonia, DYT13 type (Q86089)
- Limb-girdle muscular dystrophy 2N, POMT2 gene mutation (Q86088)
- Oromandibular dystonia (Q86087)
- Primary Dystonia DYT1 Type (Q86086)
- Primary dystonia, familial (Q86085)
- Limb dystonia (Q86084)
- Nail shedding (Q86083)
- Primary dystonia, DYT6 type (Q86082)
- Sequelae of fracture of acetabulum (Q86081)
- Laryngeal dystonia (Q86080)
- Clear cell sarcoma, of tendons and aponeuroses (Q86079)
- Primary dystonia, DYT4 type (Q86078)
- Lipoma of large intestine (Q86077)
- Greenstick fracture of shaft of radius (Q86076)
- Arthus phenomenon (Q86075)
- Autosomal dominant focal dystonia, DYT7 type (Q86074)
- Painful dorsolateral fissure of the fingertip (Q86073)
- Subungual exostosis (Q86072)
- Occipital lobe abscess (Q86071)
- Primary dystonia, DYT2 type (Q86070)
- Lipoma of small intestine (Q86069)
- Limb-girdle muscular dystrophy 2O, POMGNT1 gene mutation (Q86068)
- Limb-girdle muscular dystrophy 2L, AN05 gene mutation (Q86067)
- Limb-girdle muscular dystrophy 2J, Titin gene mutation (Q86066)
- Limb-girdle muscular dystrophy 2G, telethonin gene mutation (Q86065)
- Frontal lobe abscess (Q86064)
- Limb-girdle muscular dystrophy 2M, POMGnT1 gene mutation (Q86063)
- Temporal lobe abscess (Q86062)
- Limb-girdle muscular dystrophy 2K, protein-O-mannosyltransferase 1 transferase (Q86061)
- Limb-girdle muscular dystrophy-dystroglycanopathy C7 (Q86060)
