serw-MX  [xml]  
 


    
 Categorias DeCS

C05 Musculoskeletal Diseases .
C05.651 Muscular Diseases .
C05.651.701 Paralyses, Familial Periodic .
C05.651.701.450 Hypokalemic Periodic Paralysis .
C06 Digestive System Diseases .
C06.405 Gastrointestinal Diseases .
C06.405.469 Intestinal Diseases .
C06.405.469.637 Malabsorption Syndromes .
C06.405.469.637.506 Lactose Intolerance .
C10 Nervous System Diseases .
C10.597 Neurologic Manifestations .
C10.597.350 Dyskinesias .
C10.597.350.400 Hypokinesia .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.650 Paralyses, Familial Periodic .
C10.668.491.650.450 Hypokalemic Periodic Paralysis .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.703 Pregnancy Complications .
C13.703.844 Puerperal Disorders .
C13.703.844.506 Lactation Disorders .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.589 Lactose Intolerance .
C16.320.565.618 Metal Metabolism, Inborn Errors .
C16.320.565.618.482 Hypophosphatasia .
C16.320.565.618.711 Paralyses, Familial Periodic .
C16.320.565.618.711.550 Hypokalemic Periodic Paralysis .
C16.320.565.663 Peroxisomal Disorders .
C16.320.565.663.050 Acatalasia .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.090 Breast Diseases .
C17.800.090.937 Lactation Disorders .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.603 Malabsorption Syndromes .
C18.452.603.506 Lactose Intolerance .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.589 Lactose Intolerance .
C18.452.648.618 Metal Metabolism, Inborn Errors .
C18.452.648.618.482 Hypophosphatasia .
C18.452.648.618.711 Paralyses, Familial Periodic .
C18.452.648.618.711.550 Hypokalemic Periodic Paralysis .
C18.452.648.663 Peroxisomal Disorders .
C18.452.648.663.050 Acatalasia .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.350 Dyskinesias .
C23.888.592.350.400 Hypokinesia .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Lactose Intolerance .
Alactasia .
Dairy Product Intolerance .
Hypolactasia .
Milk Sugar Intolerance .
Intolerance, Lactose .
Malabsorption, Lactose .
Lactose Malabsorption .
1.00
 
/abnormalities .
/agenesis .
/anomalies .
/aplasia .
/atresia .
/birth defects .
/congenital defects .
/defects .
/deformities .
/hypoplasia .
/malformations .
0.60
 
Hypophosphatasia .
Hypophosphatasias .
0.56
 
Acatalasia .
Acatalasemia Japanese Type .
Acatalasemia Swiss Type .
Catalase Deficiency .
Hypocatalasia .
Takahara Disease .
Takahara's Disease .
Catalase Deficiencies .
Deficiencies, Catalase .
Deficiency, Catalase .
Disease, Takahara .
Disease, Takahara's .
Japanese Type, Acatalasemia .
Swiss Type, Acatalasemia .
Takaharas Disease .
Acatalasemia .
Hypocatalasemia .
0.53
 
Lactation Disorders .
Disorder, Lactation .
Disorders, Lactation .
Hypogalactias .
Lactation Disorder .
Hypogalactia .
0.51
 
Hypokalemic Periodic Paralysis .
HOKPP .
HYPOKPP .
HYPOPP .
Hypokalemic Periodic Paralysis, Familial .
Periodic Paralysis- Hypokalemic .
Westphall Disease .
Periodic Paralysis Hypokalemic .
Periodic Paralysis, Hypokalemic .
Periodic Paralysis- Hypokalemics .
Familial Hypokalemic Periodic Paralysis .
Paralysis, Hypokalemic Periodic .
Primary Hypokalemic Periodic Paralysis .
PRIMARY HYPOKALEMIC PERIODIC PARALYIS .
0.51
 
Hypokinesia .
Hypokinesia, Antiorthostatic .
Antiorthostatic Hypokinesia .
Antiorthostatic Hypokinesias .
Bradykinesias .
Hypokinesias, Antiorthostatic .
Bradykinesia .
Hypodynamia .
0.48