Pages that link to "Inborn errors of metabolism"
From WikiMD's Food, Medicine & Wellness Encyclopedia
The following pages link to Inborn errors of metabolism:
Displayed 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- I (← links | edit)
- Bone marrow transplantation (← links | edit)
- Category:Inborn errors of metabolism (← links | edit)
- Lesch-Nyhan syndrome (← links | edit)
- Turner's syndrome (← links | edit)
- Hyperammonemia (← links | edit)
- Congenital growth hormone deficiency (← links | edit)
- Klippel-trenaunay-weber syndrome (← links | edit)
- Mobius syndrome (← links | edit)
- Pierre robin syndrome (← links | edit)
- Somatotropin deficiency (← links | edit)
- Thyroid agenesis (← links | edit)
- Thyroid tumor (← links | edit)
- Familial medullary thyroid cancer (← links | edit)
- Adrenal hyperplasia (← links | edit)
- Fructosuria (← links | edit)
- Sclerocornea (← links | edit)
- Sanfilippo syndrome (← links | edit)
- Health topics a-z (← links | edit)
- Dictionary-of-medicine-I (← links | edit)
- Medical-dictionary-I (← links | edit)
- Encyclopedia of medicine (← links | edit)
- Health-encyclopedia-I (← links | edit)
- Template:Mucopolysaccharidoses (← links | edit)
- Amino acid metabolism, inborn errors (redirect page) (← links | edit)
- Brachydactyly type A3 (← links | edit)
- Brown syndrome (← links | edit)
- Triosephosphate isomerase deficiency (← links | edit)
- Sarcosinemia (← links | edit)
- Scheie syndrome (← links | edit)
- Purine nucleoside phosphorylase deficiency (← links | edit)
- Metastatic insulinoma (← links | edit)
- Methylmalonic acidemia (← links | edit)
- Mucopolysaccharidosis type II (← links | edit)
- Mucopolysaccharidosis type VII (← links | edit)
- Multiple carboxylase deficiency (← links | edit)
- Hurler–Scheie syndrome (← links | edit)
- Hyperlysinemia (← links | edit)
- Galactokinase deficiency (← links | edit)
- Galactose epimerase deficiency (← links | edit)
- Carnosinemia (← links | edit)
- Congenital adrenal hyperplasia (← links | edit)
- Maroteaux–Lamy syndrome (← links | edit)
- Mucopolysaccharidosis type IVA (← links | edit)
- Glutaric aciduria type 1 (← links | edit)
- Morquio syndrome (← links | edit)
- Succinic semialdehyde dehydrogenase deficiency (← links | edit)
- Hereditary multiple osteochondromas (← links | edit)
- Thyroid neoplasms (← links | edit)
- Caudal regression syndrome (← links | edit)