Pages that link to "Multiple sulfatase deficiency"
From WikiMD's Food, Medicine & Wellness Encyclopedia
The following pages link to Multiple sulfatase deficiency:
Displayed 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Angelman syndrome (← links | edit)
- Metachromatic leukodystrophy (← links | edit)
- Diamond–Blackfan anemia (← links | edit)
- List of OMIM disorder codes (← links | edit)
- List of diseases (M) (← links | edit)
- Genetic disorder (← links | edit)
- Retinitis pigmentosa (← links | edit)
- Tay-Sachs disease (← links | edit)
- Von Hippel-Lindau disease (← links | edit)
- Canavan disease (← links | edit)
- Gaucher disease (← links | edit)
- Krabbe disease (← links | edit)
- Lysosomal acid lipase deficiency (← links | edit)
- Diamond-Blackfan anemia (← links | edit)
- Gaucher's disease (← links | edit)
- Miscellaneous (← links | edit)
- X-linked spinal muscular atrophy type 2 (← links | edit)
- GM1 gangliosidoses (← links | edit)
- List of rare diseases-M (← links | edit)
- List of rare congenital and genetic diseases (← links | edit)
- List of rare skin diseases (← links | edit)
- List of rare nervous system diseases (← links | edit)
- List of rare musculoskeletal diseases (← links | edit)
- List of rare metabolic disorders (← links | edit)
- Health-encyclopedia-M (← links | edit)
- Diseases-and-disorders-M (← links | edit)
- Template:Lipid storage disorders (← links | edit)
- Template:Disorders of translation and posttranslational modification (← links | edit)
- Angiomatosis (← links | edit)
- Wolman's disease (← links | edit)
- Von hippel-lindau disease (vhl) (← links | edit)
- Leukoencephalopathy with vanishing white matter (← links | edit)
- Fragile X syndrome (← links | edit)
- Cholesteryl ester storage disease (← links | edit)
- Congenital and genetic diseases (← links | edit)
- Metabolic disorders (← links | edit)
- Musculoskeletal diseases (← links | edit)
- Skin diseases (← links | edit)
- Neuronal ceroid lipofuscinosis 2 (← links | edit)
- Ehlers-Danlos syndrome (← links | edit)
- Vascular Ehlers-Danlos syndrome (← links | edit)
- Cerebrotendineous xanthomatosis (← links | edit)
- Infantile neuronal ceroid lipofuscinosis (← links | edit)
- Classical Ehlers-Danlos syndrome (← links | edit)
- Dermatosparaxis Ehlers-Danlos syndrome (← links | edit)
- Niemann-Pick disease type B (← links | edit)
- 3-methylglutaconyl-CoA hydratase deficiency (AUH defect) (← links | edit)
- Ceroid lipofuscinosis neuronal 1 (← links | edit)
- Farber disease (← links | edit)
- Gaucher disease perinatal lethal (← links | edit)