Pages that link to "Hereditary coproporphyria"
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The following pages link to Hereditary coproporphyria:
Displayed 42 items.
- Reductive acetyl CoA Pathway (← links)
- Entner-Doudoroff Pathway (← links)
- Wikipedia:Wikiproject Metabolic Pathways/templates (← links)
- Glucose-6-phosphate (← links)
- List of fatty acid metabolism disorders (← links)
- Gangliosidosis (← links)
- Renal glycosuria (← links)
- Testpage3 (← links)
- Sialidosis (← links)
- Rasmussen's encephalitis (← links)
- Pseudo-Hurler polydystrophy (← links)
- Hepatic porphyria (← links)
- Hepatoerythropoietic porphyria (← links)
- Coproporphyria, hereditary (redirect page) (← links)
- CPO deficiency (redirect page) (← links)
- CPRO deficiency (redirect page) (← links)
- CPX deficiency (redirect page) (← links)
- HCP (redirect page) (← links)
- Aspartylglucosaminuria (← links)
- Cystathioninuria (← links)
- Catatonia (← links)
- Hemin (← links)
- ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases (← links)
- List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders (← links)
- Chromosome 3 (← links)
- The Living Textbook of Endocrinology (← links)
- The Living Textbook of Metabolic disorders (← links)
- The WikiDoc Living Textbook of Endocrinology (← links)
- The WikiDoc Living Textbook of Metabolic Disorders (← links)
- ICD-10 Chapter E: Endocrine, nutritional and metabolic diseases (← links)
- Inborn errors of purine-pyrimidine metabolism (← links)
- Hepatocellular carcinoma causes (← links)
- Porphyria classification (← links)
- Porphyria laboratory findings (← links)
- Urticaria pathophysiology (← links)
- Constipation causes (← links)
- Pancreatitis causes (← links)
- Altered mental status causes (← links)
- Template:Metabolic pathway (← links)
- Template:Metabolic pathology (← links)
- Template:Purine, pyrimidine, porphyrin, bilirubin metabolic pathology (← links)
- Template:Heme metabolism disorders (← links)