Pages that link to "Property:P78"
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The following pages link to Knowledge Architect (P78):
Displaying 50 items.
- Subclinical cystic fibrosis (Q40134) (← links)
- Cystic fibrosis (Q40135) (← links)
- Atypical cystic fibrosis (Q40136) (← links)
- Dialysis-associated amyloidosis (Q40137) (← links)
- Amyloidosis (Q40138) (← links)
- Non-neuropathic heredofamilial amyloidosis (Q40139) (← links)
- Hereditary ATTR amyloidosis (Q40140) (← links)
- Hereditary amyloidosis (Q40141) (← links)
- AA amyloidosis (Q40142) (← links)
- AL amyloidosis (Q40143) (← links)
- Volume depletion (Q40144) (← links)
- Hypovolaemia (Q40145) (← links)
- Dehydration (Q40146) (← links)
- Hyperosmolality or hypernatraemia (Q40147) (← links)
- Hypo-osmolality or hyponatraemia (Q40148) (← links)
- Anion gap metabolic acidosis (Q40149) (← links)
- Chronic respiratory acidosis (Q40150) (← links)
- 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)
