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Deficiency disease
- ... deficiency. A-alphalipoprotein neuropathy Alpha high density lipoprotein deficiency disease Analphalipoproteinemia Cholesterol thesaurismosis Familial high density lipoprotein deficiency ...
- ... the condition. Classic galactosemia Epimerase deficiency galactosemia Galactokinase deficiency disease Galactose epimerase deficiency Galactose-1-phosphate uridyl-transferase ...
- ... and symptoms of the condition. Alpha-aminoadipic semialdehyde deficiency disease Familial hyperlysinemia Lysine alpha-ketoglutarate reductase deficiency disease ...
- ... symptoms of the condition. Carbamoyl-phosphate synthase I deficiency disease Carbamyl-phosphate synthetase I deficiency disease Congenital hyperammonemia, ...
- ... symptoms of the condition. ARSA deficiency Arylsulfatase A deficiency disease Cerebral sclerosis, diffuse, metachromatic form Cerebroside sulphatase deficiency ...
- Primary Immune Deficiency Diseases (PIDDs) (National Institute of Allergy and Infectious Diseases)Immune System and Disorders/Start Here ... Immune System and Disorders ... National Institute of Allergy and Infectious Diseases ... From the National Institutes of ...
- ... Complement component 3 inactivator deficiency Hereditary factor I deficiency disease Genetic Testing Registry: Hereditary factor I deficiency disease ...
- ... of the condition. Diffuse globoid body sclerosis Galactosylceramidase deficiency disease Galactosylceramide lipidosis Galactosylcerebrosidase deficiency Galactosylsphingosine lipidosis GALC deficiency ...
- ... disease PAH deficiency Phenylalanine hydroxylase deficiency Phenylalanine hydroxylase deficiency disease PKU Genetic Testing Registry: Classical phenylketonuria Phenylketonuria National ...
- ... and symptoms of the condition. ARG1 deficiency Arginase deficiency disease Argininemia Hyperargininemia Genetic Testing Registry: Arginase deficiency Argininemia ...