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 DeCS Categories

C05 Musculoskeletal Diseases .
C05.651 Muscular Diseases .
C05.651.701 Paralyses, Familial Periodic .
C05.651.701.450 Hypokalemic Periodic Paralysis .
C07 Stomatognathic Diseases .
C07.650 Stomatognathic System Abnormalities .
C07.650.800 Tooth Abnormalities .
C07.650.800.255 Dental Enamel Hypoplasia .
C07.793 Tooth Diseases .
C07.793.700 Tooth Abnormalities .
C07.793.700.255 Dental Enamel Hypoplasia .
C10 Nervous System Diseases .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.650 Paralyses, Familial Periodic .
C10.668.491.650.450 Hypokalemic Periodic Paralysis .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.850 Stomatognathic System Abnormalities .
C16.131.850.800 Tooth Abnormalities .
C16.131.850.800.255 Dental Enamel Hypoplasia .
C16.131.894 Thyroid Dysgenesis .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.618 Metal Metabolism, Inborn Errors .
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 .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.618 Metal Metabolism, Inborn Errors .
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 .
C19 Endocrine System Diseases .
C19.874 Thyroid Diseases .
C19.874.689 Thyroid Dysgenesis .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.444 Hyperplasia .
 Synonyms & Historicals
/abnormalities .
/agenesis .
/anomalies .
/aplasia .
/atresia .
/birth defects .
/congenital defects .
/defects .
/deformities .
/hypoplasia .
/malformations .
Used with organs for congenital defects producing changes in the morphology of the organ. It is used also for abnormalities in animals. .
Thyroid Dysgenesis .
Thyroid Agenesis .
Thyroid, Ectopic .
Agenesis, Thyroid .
Dysgenesis, Thyroid .
Ectopic Thyroid .
Ectopic Thyroids .
Hypoplasia, Thyroid .
Thyroids, Ectopic .
Thyroid Hypoplasia .
Defective development of the THYROID GLAND. This concept includes thyroid agenesis (aplasia), hypoplasia, or an ectopic gland. Clinical signs usually are those of CONGENITAL HYPOTHYROIDISM. .
Dental Enamel Hypoplasia .
Enamel Agenesis .
Enamel Hypoplasia, Dental .
Hypoplasia, Dental Enamel .
Hypoplastic Enamel .
Molar Incisor Hypomineralization .
Ageneses, Enamel .
Agenesis, Enamel .
Enamel Ageneses .
Enamel Hypoplasias .
Enamel, Hypoplastic .
Hypomineralization, Molar Incisor .
Hypoplasia, Enamel .
Hypoplasias, Enamel .
Enamel Hypoplasia .
An acquired or hereditary condition due to deficiency in the formation of tooth enamel (AMELOGENESIS). It is usually characterized by defective, thin, or malformed DENTAL ENAMEL. Risk factors for enamel hypoplasia include gene mutations, nutritional deficiencies, diseases, and environmental factors. .
Hypokalemic Periodic Paralysis .
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 .
An autosomal dominant familial disorder characterized by recurrent episodes of skeletal muscle weakness associated with falls in serum potassium levels. The condition usually presents in the first or second decade of life with attacks of trunk and leg paresis during sleep or shortly after awakening. Symptoms may persist for hours to days and generally are precipitated by exercise or a meal high in carbohydrates. (Adams et al., Principles of Neurology, 6th ed, p1483) .
Hyperplasia .
Hyperplasias .
An increase in the number of cells in a tissue or organ without tumor formation. It differs from HYPERTROPHY, which is an increase in bulk without an increase in the number of cells. .
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 .
A rare autosomal recessive disorder resulting from the absence of CATALASE activity. Though usually asymptomatic, a syndrome of oral ulcerations and gangrene may be present. .