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 DeCS Categories

C06 Digestive System Diseases .
C06.405 Gastrointestinal Diseases .
C06.405.748 Stomach Diseases .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.550 Neuronal Ceroid-Lipofuscinoses .
C10.597 Neurologic Manifestations .
C10.597.606 Neurobehavioral Manifestations .
C10.597.606.643 Intellectual Disability .
C10.597.606.643.455 Mental Retardation, X-Linked .
C10.597.606.643.455.562 Glycogen Storage Disease Type IIb .
C14 Cardiovascular Diseases .
C14.280 Heart Diseases .
C14.280.238 Cardiomyopathies .
C14.280.238.458 Glycogen Storage Disease Type IIb .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.201 Glycogen Storage Disease Type IIb .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.600 Neuronal Ceroid-Lipofuscinoses .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.435 Lysosomal Storage Diseases, Nervous System .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.449 Glycogen Storage Disease .
C16.320.565.202.449.510 Glycogen Storage Disease Type IIb .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.509 Neuronal Ceroid-Lipofuscinoses .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.435 Lysosomal Storage Diseases, Nervous System .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.687 Lipidoses .
C18.452.584.687.509 Neuronal Ceroid-Lipofuscinoses .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.449 Glycogen Storage Disease .
C18.452.648.202.449.510 Glycogen Storage Disease Type IIb .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.509 Neuronal Ceroid-Lipofuscinoses .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Lysosomal Storage Diseases .
Disease, Lysosomal Storage .
Diseases, Lysosomal Storage .
Disorder, Lysosomal Enzyme .
Disorders, Lysosomal Enzyme .
Enzyme Disorder, Lysosomal .
Enzyme Disorders, Lysosomal .
Lysosomal Enzyme Disorder .
Lysosomal Storage Disease .
Lysosomal Enzyme Disorders .
Inborn errors of metabolism characterized by defects in specific lysosomal hydrolases and resulting in intracellular accumulation of unmetabolized substrates. .
1.00
351351
 
Lysosomal Storage Diseases, Nervous System .
Lysosomal Enzyme Disorders, Nervous System .
Nervous System Lysosomal Enzyme Disorders .
Nervous System Lysosomal Storage Diseases .
A group of enzymatic disorders affecting the nervous system and to a variable degree the skeletal system, lymphoreticular system, and other organs. The conditions are marked by an abnormal accumulation of catabolic material within lysosomes. .
0.80
183
 
Glycogen Storage Disease Type IIb .
Antopol Disease .
Danon Disease .
Glycogen Storage Cardiomyopathy .
Glycogen Storage Disease IIb .
Glycogen Storage Disease Limited to the Heart .
Glycogen Storage Disease Type 2B .
Lysosomal Glycogen Storage Disease with Normal Acid Maltase .
Lysosomal Glycogen Storage Disease without Acid Maltase Deficiency .
Pseudoglycogenosis 2 .
Pseudoglycogenosis II .
Vacuolar Cardiomyopathy and Myopathy, X-linked .
X-Linked Vacuolar Cardiomyopathy and Myopathy .
Cardiomyopathies, Glycogen Storage .
Cardiomyopathy, Glycogen Storage .
Disease, Antopol .
Glycogen Storage Cardiomyopathies .
Pseudoglycogenosis 2s .
Pseudoglycogenosis IIs .
Vacuolar Cardiomyopathy and Myopathy, X linked .
X Linked Vacuolar Cardiomyopathy and Myopathy .
An X-linked dominant multisystem disorder resulting in cardiomyopathy, myopathy and INTELLECTUAL DISABILITY. It is caused by mutation in the gene encoding LYSOSOMAL-ASSOCIATED MEMBRANE PROTEIN 2. .
0.63
 
Neuronal Ceroid-Lipofuscinoses .
Adult Neuronal Ceroid Lipofuscinosis .
Amaurotic Idiocy, Adult Type .
Batten-Mayou Disease .
Batten-Spielmeyer-Vogt Disease .
CLN3-Related Neuronal Ceroid-Lipofuscinosis .
CLN4A .
CLN4B .
Ceroid Lipofuscinosis, Neuronal 3, Juvenile .
Ceroid Lipofuscinosis, Neuronal 4 .
Ceroid Lipofuscinosis, Neuronal, 3 .
Ceroid Lipofuscinosis, Neuronal, 4A, Autosomal Recessive .
Ceroid Lipofuscinosis, Neuronal, 4B, Autosomal Dominant .
Ceroid Lipofuscinosis, Neuronal, Parry Type .
Ceroid Storage Disease .
Infantile Neuronal Ceroid Lipofuscinosis .
Juvenile Batten Disease .
Juvenile Cerebroretinal Degeneration .
Juvenile Neuronal Ceroid Lipofuscinosis .
Kuf's Disease .
Kufs Disease Autosomal Recessive .
Kufs Disease, Autosomal Dominant .
Kufs Disease, Autosomal Recessive .
Kufs Type Neuronal Ceroid Lipofuscinosis .
Late-Infantile Neuronal Ceroid Lipofuscinosis .
Lipofuscin Storage Disease .
Lipofuscinosis, Neuronal Ceroid .
Neuronal Ceroid Lipofuscinosis .
Neuronal Ceroid Lipofuscinosis Juvenile Type .
Neuronal Ceroid Lipofuscinosis, Adult .
Neuronal Ceroid Lipofuscinosis, Adult Type .
Neuronal Ceroid Lipofuscinosis, Infantile .
Neuronal Ceroid Lipofuscinosis, Juvenile .
Neuronal Ceroid Lipofuscinosis, Late Infantile .
Neuronal Ceroid Lipofuscinosis, Late-Infantile .
Neuronal Ceroid-Lipofuscinosis .
Spielmeyer-Sjogren Disease .
Vogt Spielmeyer Disease .
Vogt-Spielmeyer Disease .
Batten Disease, Juvenile .
Batten Diseases, Juvenile .
Batten Mayou Disease .
Batten Spielmeyer Vogt Disease .
CLN3 Related Neuronal Ceroid Lipofuscinosis .
CLN3-Related Neuronal Ceroid-Lipofuscinoses .
CLN4As .
Cerebroretinal Degeneration, Juvenile .
Cerebroretinal Degenerations, Juvenile .
Ceroid Lipofuscinosis, Neuronal .
Ceroid Storage Diseases .
Ceroid-Lipofuscinoses, CLN3-Related Neuronal .
Ceroid-Lipofuscinosis, CLN3-Related Neuronal .
Disease, Ceroid Storage .
Disease, Juvenile Batten .
Disease, Kuf's .
Disease, Lipofuscin Storage .
Disease, Spielmeyer-Sjogren .
Disease, Vogt Spielmeyer .
Disease, Vogt-Spielmeyer .
Diseases, Ceroid Storage .
Diseases, Juvenile Batten .
Diseases, Lipofuscin Storage .
Jansky Bielschowsky Disease .
Juvenile Batten Diseases .
Juvenile Cerebroretinal Degenerations .
Kuf Disease .
Lipofuscin Storage Diseases .
Neuronal Ceroid Lipofuscinoses .
Neuronal Ceroid-Lipofuscinoses, CLN3-Related .
Neuronal Ceroid-Lipofuscinosis, CLN3-Related .
Santavuori Haltia Disease .
Spielmeyer Disease, Vogt .
Spielmeyer Sjogren Disease .
Spielmeyer Vogt Disease .
Storage Disease, Ceroid .
Storage Disease, Lipofuscin .
Storage Diseases, Ceroid .
Storage Diseases, Lipofuscin .
Batten Disease .
Ceroid-Lipofuscinosis, Neuronal .
Jansky-Bielschowsky Disease .
Kufs Disease .
Santavuori-Haltia Disease .
Spielmeyer-Vogt Disease .
Neuronal Ceroid-Lipofuscinosis .
CEROID-LIPOFUSCINOSIS .
BATTEN-SPIELMEYER-VOGT DISEASE .
LIPOFUSCINOSIS, NEURONAL CEROID .
A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure. .
0.60
151701
 
Stomach Diseases .
Gastric Diseases .
Disease, Gastric .
Disease, Stomach .
Diseases, Gastric .
Diseases, Stomach .
Gastric Disease .
Stomach Disease .
Pathological processes involving the STOMACH. .
0.60
21810996