Pages that link to "Property:P68"
From determinar.ia.br - Determine suas informações
The following pages link to Canonical URI (P68):
Displaying 50 items.
- Primary hyperoxaluria type 1 (Q40060) (← links)
- Disorders of glyoxylate metabolism (Q40061) (← links)
- Disorders of cholesterol synthesis (Q40062) (← links)
- Neutral lipid storage disease (Q40063) (← links)
- Inborn errors of lipid metabolism (Q40064) (← links)
- Inborn errors of sterol metabolism (Q40065) (← links)
- Bile acid synthesis defect with cholestasis (Q40066) (← links)
- Liver disease due to disorders of lysosomal storage (Q40067) (← links)
- Pelizaeus-Merzbacher disease (Q40068) (← links)
- Metachromatic leukodystrophy (Q40069) (← links)
- Fabry disease (Q40070) (← links)
- Gangliosidosis (Q40071) (← links)
- Sphingolipidosis (Q40072) (← links)
- Neuronal ceroid lipofuscinosis (Q40073) (← links)
- Tendinous xanthoma (Q40074) (← links)
- Plane xanthoma (Q40075) (← links)
- Cutaneous or subcutaneous xanthomata (Q40076) (← links)
- Mucopolysaccharidosis type 1 (Q40077) (← links)
- Mucopolysaccharidosis type 2 (Q40078) (← links)
- Mucopolysaccharidosis type 6 (Q40079) (← links)
- Mucopolysaccharidosis type 4 (Q40080) (← links)
- Mucopolysaccharidosis (Q40081) (← links)
- Disorders of sialic acid metabolism (Q40082) (← links)
- Disorders of protein O-glycosylation (Q40083) (← links)
- Disorders of multiple glycosylation or other pathways (Q40084) (← links)
- Disorders of protein N-glycosylation (Q40085) (← links)
- Oligosaccharidosis (Q40086) (← links)
- Glycoproteinosis (Q40087) (← links)
- Mucolipidosis (Q40088) (← links)
- Primary hypercholesterolaemia (Q40089) (← links)
- Hypertriglyceridaemia (Q40090) (← links)
- Eruptive xanthoma (Q40091) (← links)
- Tuberous xanthoma (Q40092) (← links)
- Mixed hyperlipidaemia (Q40093) (← links)
- Hyperlipoproteinaemia (Q40094) (← links)
- Hyperalphalipoproteinaemia (Q40095) (← links)
- Secondary hypercholesterolaemia (Q40096) (← links)
- Hypercholesterolaemia (Q40097) (← links)
- Hypobetalipoproteinaemia (Q40098) (← links)
- Hypoalphalipoproteinaemia (Q40099) (← links)
- Hypolipoproteinaemia (Q40100) (← links)
- 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)
