Pages that link to "Property:P89"
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The following pages link to Linked ICD 10 (P89):
Displaying 50 items.
- Acidosis (Q40151) (← links)
- Acute respiratory acidosis (Q40152) (← links)
- Alkalosis (Q40153) (← links)
- Mixed disorder of acid-base balance (Q40154) (← links)
- Hyperkalaemia (Q40155) (← links)
- Hypokalaemia (Q40156) (← links)
- Fluid overload (Q40157) (← links)
- Alpha-1-antitrypsin deficiency (Q40158) (← links)
- Lipoatrophy or lipodystrophy (Q40159) (← links)
- Genetic lipodystrophy (Q40160) (← links)
- Localised lipoatrophy or lipodystrophy (Q40161) (← links)
- Congenital generalised lipodystrophy (Q40162) (← links)
- Acquired partial lipodystrophy (Q40163) (← links)
- Tumour lysis syndrome (Q40165) (← links)
- Mitochondrial protein translation defects (Q40166) (← links)
- Mitochondrial protein import disorders (Q40167) (← links)
- Disorders of catecholamine synthesis (Q40168) (← links)
- Mitochondrial DNA depletion syndromes (Q40169) (← links)
- Disorders of cobalamin metabolism or transport (Q40170) (← links)
- Disorders of vitamin D metabolism or transport (Q40171) (← links)
- Disorders of gamma aminobutyric acid metabolism (Q40172) (← links)
- Disorders of biogenic amine metabolism (Q40173) (← links)
- Hypophosphataemic rickets (Q40174) (← links)
- Disorders of folate metabolism or transport (Q40175) (← links)
- Hypocalcaemic vitamin D resistant rickets (Q40176) (← links)
- Disorders of mitochondrial membrane transport (Q40177) (← links)
- Inborn errors of neurotransmitter metabolism (Q40178) (← links)
- Disorders of vitamin or non-protein cofactor absorption or transport (Q40179) (← links)
- Disorders of mitochondrial oxidative phosphorylation (Q40180) (← links)
- Trimethylaminuria (Q40181) (← links)
- Disorders of pyridoxine metabolism (Q40182) (← links)
- Hypocalcaemic vitamin D dependent rickets (Q40183) (← links)
- Isolated ATP synthase deficiency (Q40184) (← links)
- Disorders of pterin metabolism (Q40185) (← links)
- Disorders of the citric acid cycle (Q40186) (← links)
- Coenzyme Q10 deficiency (Q40187) (← links)
- Mitochondrial substrate carrier disorders (Q40188) (← links)
- Multiple mitochondrial DNA deletion syndromes (Q40189) (← links)
- Peroxisomal diseases (Q40190) (← links)
- Disorders of peptide metabolism (Q40191) (← links)
- Inborn errors of energy metabolism (Q40192) (← links)
- Inborn errors of amino acid or other organic acid metabolism (Q40193) (← links)
- Liver diseases due to disorders of amino acid metabolism (Q40194) (← links)
- Liver diseases due to disorders of porphyrin or bilirubin metabolism or transport (Q40195) (← links)
- Inborn errors of glycosylation or other specified protein modification (Q40196) (← links)
- Disorders of carbohydrate absorption or transport (Q40197) (← links)
- Lysosomal diseases (Q40198) (← links)
- Metabolic or transporter liver disease (Q40199) (← links)
- Liver diseases due to urea cycle defects (Q40200) (← links)
- Liver diseases due to mitochondrial disorders (Q40201) (← links)
