Pages that link to "Diseases Database"

The following pages link to Diseases Database:

Displaying 50 items.

• Benign familial neonatal convulsions (← links)
• Beta-ketothiolase deficiency (← links)
• Birt-Hogg-Dubé syndrome (← links)
• CADASIL (← links)
• Canavan disease (← links)
• Carbamoyl phosphate synthetase I deficiency (← links)
• Cardiofaciocutaneous syndrome (← links)
• Carnitine palmitoyltransferase I deficiency (← links)
• Carnitine palmitoyltransferase II deficiency (← links)
• Carpenter syndrome (← links)
• Charcot-Marie-Tooth disease (← links)
• Chronic granulomatous disease (← links)
• Citrullinemia (← links)
• Cockayne syndrome (← links)
• Coffin-Lowry syndrome (← links)
• Cohen syndrome (← links)
• Congenital disorder of glycosylation (← links)
• Cornelia de Lange Syndrome (← links)
• Costello syndrome (← links)
• Crouzon syndrome (← links)
• Darier's disease (← links)
• Dejerine Sottas syndrome (← links)
• Diamond-Blackfan anemia (← links)
• Diastrophic dysplasia (← links)
• Duane-radial ray syndrome (← links)
• Dubowitz syndrome (← links)
• Duchenne muscular dystrophy (← links)
• Edwards syndrome (← links)
• Ellis-van Creveld syndrome (← links)
• Emery-Dreifuss muscular dystrophy (← links)
• Essential fructosuria (← links)
• Facioscapulohumeral muscular dystrophy (← links)
• Familial atrial fibrillation (← links)
• Familial hemiplegic migraine (← links)
• Feingold syndrome (← links)
• Fragile X syndrome (← links)
• Friedreich's ataxia (← links)
• Galactose-1-phosphate uridylyltransferase galactosemia (← links)
• Gardner's syndrome (← links)
• Gitelman syndrome (← links)
• Glucose-galactose malabsorption (← links)
• Glutathione synthetase deficiency (← links)
• Greig cephalopolysyndactyly syndrome (← links)
• Guanidinoacetate methyltransferase deficiency (← links)
• Hereditary coproporphyria (← links)
• Hereditary elliptocytosis (← links)
• Hereditary multiple exostoses (← links)
• Histidinemia (← links)
• Holocarboxylase synthetase deficiency (← links)
• Holt-Oram syndrome (← links)