Pages that link to "Property:P89"
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The following pages link to Linked ICD 10 (P89):
Displaying 50 items.
- Disorders of lipid absorption or transport (Q40101) (← links)
- Disorders of purine metabolism (Q40102) (← links)
- Disorders of nucleotide metabolism (Q40103) (← links)
- Inborn errors of purine, pyrimidine or nucleotide metabolism (Q40104) (← links)
- Disorders of pyrimidine metabolism (Q40105) (← links)
- Lesch-Nyhan syndrome (Q40106) (← links)
- Xanthinuria (Q40107) (← links)
- Inborn errors of porphyrin or heme metabolism (Q40108) (← links)
- Porphyrias (Q40109) (← links)
- Erythropoietic porphyrias (Q40110) (← links)
- Porphyria cutanea tarda (Q40111) (← links)
- Variegate porphyria (Q40112) (← links)
- Pseudoporphyria (Q40113) (← links)
- Gilbert syndrome (Q40114) (← links)
- Crigler-Najjar syndrome (Q40115) (← links)
- Dubin-Johnson syndrome (Q40116) (← links)
- Disorders of bilirubin metabolism or excretion (Q40117) (← links)
- Liver diseases due to disorders of mineral metabolism (Q40118) (← links)
- Wilson disease (Q40119) (← links)
- Disorders of copper metabolism (Q40120) (← links)
- Disorders of iron metabolism (Q40121) (← links)
- Iron overload diseases (Q40122) (← links)
- Disorders of zinc metabolism (Q40123) (← links)
- Acrodermatitis enteropathica (Q40124) (← links)
- Zinc deficiency syndromes (Q40125) (← links)
- Disorders of phosphorus metabolism or phosphatases (Q40126) (← links)
- Hypermagnesaemia (Q40127) (← links)
- Disorders of magnesium metabolism (Q40128) (← links)
- Disorders of calcium metabolism (Q40129) (← links)
- Disorders of chloride metabolism (Q40130) (← links)
- Disorders of sodium metabolism (Q40131) (← links)
- Disorders of mineral absorption or transport (Q40132) (← links)
- Classical cystic fibrosis (Q40133) (← links)
- 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)
