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Mucocutaneous Lymph Node Disease
Mucocutaneous lymph node disease
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Vascular-related cutaneous conditions
Purpura, schoenlein-henoch
Vasculitis
Polyarteritis
Systemic vasculitis
Takayasu
Temporal arteritis
Cardiology
(9)
Myocardial contusion
Myxoma
Coronary arteries
Echocardiogram
Coronary artery aneurysm
Coronary artery aneurysm
Myocarditis
Pericarditis
Cardiomyopathy
Takayasu
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Pediatrics
Hyperostosis, cortical, congenital
Purpura, schoenlein-henoch
Diseases and disorders
(45)
Mucopolysa- ccharidosis iii
Myotonia atrophica
Munchausens syndrome
Myxomatous mitral valve
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis iv
Muscle fasciculation
Mucolipidoses
Mucopolysa- ccharidosis, type I
Cytomegalovirus
Lupus erythematosus, cutaneous
Glossopharyngeal nerve diseases
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Aneurysms
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Intervertebral disk displacement
Rosenthal syndrome
Optic neuropathy, ischemic
Galactosemias
Brachial plexus neuropathies
Swollen lymph nodes
Conjunctivitis
Fever
Aseptic meningitis
Edematous
Myxoma
Purpura, schoenlein-henoch
Hyperostosis, cortical, congenital
Vasculitis
Coronary artery aneurysm
Myocarditis
Polyarteritis
Pericarditis
Takayasu
Temporal arteritis
Cardiomyopathy
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Genetic disorders
(11)
Myoclonic Epilepsy with Ragged Red Fibers
Multiple lentigines syndrome
Adrenoleuk- odystrophy
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis iv
Mucolipidoses
Mucopolysa- ccharidosis, type I
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Galactosemias
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Lysosomal storage diseases
(40)
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
I-cell disease
Leukodystrophy, globoid cell
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Mucolipidoses
Mucolipidosis type IV
Mucopolysa- ccharidosis
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis, type I
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
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Symptoms
(15)
Movement dysfunctional
Motormental retardation
Muscle function loss
Uncoordinated movement
Bright red chapped or cracked lips
Bright red chapped or cracked lips
Strawberry tongue
Arthralgia
Red palms
High fever
Reddening
Rash
Muscle fasciculation
Swollen lymph nodes
Inflammation
Fever
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Signs and tests
(10)
Arthritis
C-reactive protein
Chest radiograph
Complete blood count
ESR
ESR
Electrocardiography
Protein in the urine
Serum albumin
Urinalysis
Echocardiography
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See also
(20)
Monorchism
Tomisaku Kawasaki
Vasospasm, intracranial
IVIg
Gamma globulin
Gamma globulin
Lymph nodes
Mucocutaneous
Autoimmune disease
Myocardial infarction
Reye's syndrome
Mucous membranes
Braunwald
Jett Travolta
Hamaoka
Lymph
The Disease
Inflammation
Diagnostic criteria
Red eyes
Estrogen receptor
more...
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