Pages that link to "Property:P70"
From determinar.ia.br - Determine suas informações
The following pages link to Canary Token (P70):
Displaying 50 items.
- 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)
- 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)
