Pages that link to "Congenital disorder of glycosylation"
Showing 50 items.
- Charcot–Marie–Tooth disease (links | edit)
- Genetic disorder (links | edit)
- Crohn's disease (links | edit)
- Glycogen storage disease (links | edit)
- Glycoprotein (links | edit)
- Congenital disorder of glycosylation (transclusion) (links | edit)
- Mannose (links | edit)
- Microcephaly (links | edit)
- Macrocephaly (links | edit)
- Hereditary spastic paraplegia (links | edit)
- List of diseases (C) (links | edit)
- Long QT syndrome (links | edit)
- CDG (links | edit)
- Limb–girdle muscular dystrophy (links | edit)
- Glycosylation (links | edit)
- Phosphoglucomutase (links | edit)
- Lysosomal storage disease (links | edit)
- Fructose malabsorption (links | edit)
- Hyperinsulinemic hypoglycemia (links | edit)
- Hypotonia (links | edit)
- Alpha-mannosidosis (links | edit)
- Hereditary multiple exostoses (links | edit)
- Cystinuria (links | edit)
- Pendred syndrome (links | edit)
- Diastrophic dysplasia (links | edit)
- Atelosteogenesis, type II (links | edit)
- Exophthalmos (links | edit)
- Fuchs' dystrophy (links | edit)
- Gitelman syndrome (links | edit)
- Spinocerebellar ataxia (links | edit)
- Microtia (links | edit)
- Hartnup disease (links | edit)
- Chédiak–Higashi syndrome (links | edit)
- Sialidosis (links | edit)
- Salla disease (links | edit)
- Lysinuric protein intolerance (links | edit)
- List of congenital disorders (links | edit)
- Leukocyte adhesion deficiency (links | edit)
- Hereditary elliptocytosis (links | edit)
- Achondrogenesis type 1B (links | edit)
- Mucolipidosis (links | edit)
- African iron overload (links | edit)
- Mannosidosis (links | edit)
- Glycoproteinosis (links | edit)
- Nonsyndromic deafness (links | edit)
- Hermansky–Pudlak syndrome (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Choroideremia (links | edit)
- Cohen syndrome (links | edit)
- Autosomal recessive multiple epiphyseal dysplasia (links | edit)