The following pages link to Allan–Herndon–Dudley syndrome
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Genetic disorder (links | edit)
- List of neurological conditions and disorders (links | edit)
- Crohn's disease (links | edit)
- Congenital disorder of glycosylation (links | edit)
- Hereditary spastic paraplegia (links | edit)
- List of diseases (A) (links | edit)
- Fructose malabsorption (links | edit)
- Hyperinsulinemic hypoglycemia (links | edit)
- Cystinuria (links | edit)
- Pendred syndrome (links | edit)
- Diastrophic dysplasia (links | edit)
- Atelosteogenesis, type II (links | edit)
- Fuchs' dystrophy (links | edit)
- Gitelman syndrome (links | edit)
- Hartnup disease (links | edit)
- Salla disease (links | edit)
- Lysinuric protein intolerance (links | edit)
- Hereditary elliptocytosis (links | edit)
- Achondrogenesis type 1B (links | edit)
- African iron overload (links | edit)
- Nonsyndromic deafness (links | edit)
- Autosomal recessive multiple epiphyseal dysplasia (links | edit)
- Acrodermatitis enteropathica (links | edit)
- Testicular microlithiasis (links | edit)
- Solute carrier family (links | edit)
- Multiple epiphyseal dysplasia (links | edit)
- Episodic ataxia (links | edit)
- Thyroid dyshormonogenesis (links | edit)
- Allan Herndon syndrome (redirect page) (links | edit)
- Arterial tortuosity syndrome (links | edit)
- Renal glycosuria (links | edit)
- Allan-Herndon syndrome (redirect page) (links | edit)
- Mental retardation, X-linked, with hypotonia (redirect page) (links | edit)
- Monocarboxylate transporter 8 (MCT8) deficiency (redirect page) (links | edit)
- Monocarboxylate transporter 8 deficiency (redirect page) (links | edit)
- MCT8 deficiency (redirect page) (links | edit)
- GLUT1 deficiency (links | edit)
- Glucose-galactose malabsorption (links | edit)
- Monocarboxylate transporter 8 (links | edit)
- Mitochondrial pyruvate carrier 2 (links | edit)
- Monocarboxylate transporter 1 (links | edit)
- Fanconi–Bickel syndrome (links | edit)
- Inborn errors of carbohydrate metabolism (links | edit)
- Iminoglycinuria (links | edit)
- William Allan (geneticist) (links | edit)
- Ichthyosis prematurity syndrome (links | edit)
- Congenital disorder of glycosylation type IIc (links | edit)
- Allan-Herndon-Dudley syndrome (redirect page) (links | edit)
- List of OMIM disorder codes (links | edit)
- SLC17A3 (links | edit)