serw-MX  [xml]  
 


    
 DeCS Categories

C05 Musculoskeletal Diseases .
C05.660 Musculoskeletal Abnormalities .
C05.660.207 Craniofacial Abnormalities .
C05.660.207.325 Donohue Syndrome .
C08 Respiratory Tract Diseases .
C08.381 Lung Diseases .
C08.381.677 Pneumonia .
C08.381.677.529 Pneumonia, Aspiration .
C08.730 Respiratory Tract Infections .
C08.730.610 Pneumonia .
C08.730.610.529 Pneumonia, Aspiration .
C09 Otorhinolaryngologic Diseases .
C09.218 Ear Diseases .
C09.218.568 Labyrinth Diseases .
C09.218.568.217 Endolymphatic Hydrops .
C09.218.568.217.500 Meniere Disease .
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 .
C10.228.140.163.100.540 Menkes Kinky Hair Syndrome .
C10.597 Neurologic Manifestations .
C10.597.606 Neurobehavioral Manifestations .
C10.597.606.643 Intellectual Disability .
C10.597.606.643.455 Mental Retardation, X-Linked .
C10.597.606.643.455.687 Menkes Kinky Hair Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.313 Donohue Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.215 Donohue Syndrome .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.500 Mental Retardation, X-Linked .
C16.320.322.500.687 Menkes Kinky Hair Syndrome .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.525 Mental Retardation, X-Linked .
C16.320.400.525.687 Menkes Kinky Hair Syndrome .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.540 Menkes Kinky Hair Syndrome .
C16.320.565.618 Metal Metabolism, Inborn Errors .
C16.320.565.618.590 Menkes Kinky Hair Syndrome .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.329 Hair Diseases .
C17.800.329.968 Menkes Kinky Hair Syndrome .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.540 Menkes Kinky Hair Syndrome .
C18.452.394 Glucose Metabolism Disorders .
C18.452.394.750 Diabetes Mellitus .
C18.452.394.750.654 Donohue Syndrome .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.540 Menkes Kinky Hair Syndrome .
C18.452.648.618 Metal Metabolism, Inborn Errors .
C18.452.648.618.590 Menkes Kinky Hair Syndrome .
C19 Endocrine System Diseases .
C19.246 Diabetes Mellitus .
C19.246.537 Donohue Syndrome .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Meniere Disease .
Auditory Vertigo .
Aural Vertigo .
Ménière Disease .
Ménière's Disease .
Ménière's Vertigo .
Otogenic Vertigo .
Auditory Vertigos .
Disease, Meniere .
Disease, Meniere's .
Disease, Ménière .
Disease, Ménière's .
Diseases, Ménière .
Diseases, Ménière's .
Meniere Syndrome .
Menieres Disease .
Menieres Syndrome .
Ménière Diseases .
Ménière Vertigo .
Ménière's Diseases .
Ménière's Vertigos .
Ménières Disease .
Ménières Vertigo .
Otogenic Vertigos .
Syndrome, Meniere's .
Vertigo, Auditory .
Vertigo, Ménière's .
Vertigo, Otogenic .
Vertigos, Auditory .
Vertigos, Ménière's .
Vertigos, Otogenic .
Meniere's Disease .
Vertigo, Aural .
Meniere's Syndrome .
Meniere's Disease n .
A disease of the inner ear (LABYRINTH) that is characterized by fluctuating SENSORINEURAL HEARING LOSS; TINNITUS; episodic VERTIGO; and aural fullness. It is the most common form of endolymphatic hydrops. .
1.00
1135739
 
Menkes Kinky Hair Syndrome .
Congenital Hypocupremia .
Copper Transport Disease .
Kinky Hair Disease .
Menkea Syndrome .
Menkes Disease .
Menkes' Disease .
Steely Hair Disease .
X-Linked Copper Deficiency .
Congenital Hypocupremias .
Copper Deficiencies, X-Linked .
Copper Deficiency, X-Linked .
Copper Transport Diseases .
Deficiencies, X-Linked Copper .
Deficiency, X-Linked Copper .
Disease, Copper Transport .
Disease, Steely Hair .
Diseases, Copper Transport .
Diseases, Kinky Hair .
Diseases, Menkes' .
Diseases, Steely Hair .
Hair Diseases, Kinky .
Hair Diseases, Steely .
Hypocupremias, Congenital .
Kinky Hair Diseases .
Menkea Syndromes .
Menkes' Diseases .
Steely Hair Diseases .
Steely Hair Syndromes .
Syndrome, Menkea .
Syndrome, Steely Hair .
Syndromes, Menkea .
Syndromes, Steely Hair .
Transport Disease, Copper .
Transport Diseases, Copper .
X Linked Copper Deficiency .
X-Linked Copper Deficiencies .
Menkes Syndrome .
Steely Hair Syndrome .
Kinky Hair Syndrome .
Hypocupremia, Congenital .
An inherited disorder of copper metabolism transmitted as an X-linked trait and characterized by the infantile onset of HYPOTHERMIA, feeding difficulties, hypotonia, SEIZURES, bony deformities, pili torti (twisted hair), and severely impaired intellectual development. Defective copper transport across plasma and endoplasmic reticulum membranes results in copper being unavailable for the synthesis of several copper containing enzymes, including PROTEIN-LYSINE 6-OXIDASE; CERULOPLASMIN; and SUPEROXIDE DISMUTASE. Pathologic changes include defects in arterial elastin, neuronal loss, and gliosis. (From Menkes, Textbook of Child Neurology, 5th ed, p125) .
0.73
20953
 
Pneumonia, Aspiration .
Gastric Acid Aspiration Syndrome .
Mendelson Syndrome .
Mendelson's Syndrome .
Acid Aspiration Syndromes .
Aspiration Pneumonias .
Mendelsons Syndrome .
Pneumonias, Aspiration .
Syndrome, Acid Aspiration .
Syndrome, Mendelson .
Syndrome, Mendelson's .
Syndromes, Acid Aspiration .
Acid Aspiration Syndrome .
Aspiration Pneumonia .
A type of lung inflammation resulting from the aspiration of food, liquid, or gastric contents into the upper RESPIRATORY TRACT. .
0.69
1245119
 
Donohue Syndrome .
Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, And Somatic Abnormalities .
Leprechaunisms .
Rabson Mendenhall Syndrome .
Syndrome, Donohue .
Syndrome, Mendenhall .
Syndrome, Rabson-Mendenhall .
Leprechaunism .
Mendenhall Syndrome .
Rabson-Mendenhall Syndrome .
Rare autosomal recessive syndrome of extreme insulin resistance due to mutations in the binding domain of INSULIN RECEPTOR. Clinical features include severe intrauterine and postnatal growth restriction, characteristic dysmorphic FACIES; HIRSUTISM; VIRILIZATION; multiple endocrine abnormalities, and early death. .
0.67
147