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 Categorias DeCS

C10 Nervous System Diseases .
C10.597 Neurologic Manifestations .
C10.597.606 Neurobehavioral Manifestations .
C10.597.606.643 Intellectual Disability .
C10.597.606.643.180 Cri-du-Chat Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.262 Cri-du-Chat Syndrome .
C16.131.260 Chromosome Disorders .
C16.131.260.190 Cri-du-Chat Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.180 Chromosome Disorders .
C16.320.180.190 Cri-du-Chat Syndrome .
C16.320.382 Hereditary Autoinflammatory Diseases .
C16.320.382.500 Cryopyrin-Associated Periodic Syndromes .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.827 Skin Diseases, Genetic .
C17.800.827.368 Hereditary Autoinflammatory Diseases .
C17.800.827.368.500 Cryopyrin-Associated Periodic Syndromes .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
C23.550.288.500 Syndrome .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Cryopyrin-Associated Periodic Syndromes .
CINCA .
Chronic Infantile Neurologic, Cutaneous, and Articular Syndrome .
Chronic Neurologic Cutaneous and Articular Syndrome .
Chronic Neurologic, Cutaneous, and Articular Syndrome .
Chronic, Infantile, Neurological, Cutaneous, Articular Syndrome .
Cold Urticaria, Familial .
Cold-Induced Autoinflammatory Syndrome, Familial .
FCAS1 .
Familial Cold Autoinflammatory Syndrome 1 .
Familial Cold-Induced Autoinflammatory Syndrome .
IOMID Syndrome .
Prieur-Griscelli Syndrome .
UDA Syndrome .
Urticaria, Deafness and Amyloidosis .
Urticaria-Deafness-Amyloidosis Syndrome .
Cold Induced Autoinflammatory Syndrome, Familial .
Cold Urticarias, Familial .
Cryopyrin Associated Periodic Syndromes .
Cryopyrin-Associated Periodic Syndrome .
Cryopyrinopathies .
Familial Cold Induced Autoinflammatory Syndrome .
Familial Cold Urticarias .
IOMID Syndromes .
Muckle Wells Syndrome .
Multisystem Inflammatory Disease, Neonatal Onset .
Prieur Griscelli Syndrome .
Prieur-Griscelli Syndromes .
Syndrome, IOMID .
Syndrome, Muckle-Wells .
Syndrome, Prieur-Griscelli .
Syndrome, UDA .
Syndrome, Urticaria-Deafness-Amyloidosis .
Syndromes, IOMID .
Syndromes, Prieur-Griscelli .
Syndromes, UDA .
Syndromes, Urticaria-Deafness-Amyloidosis .
UDA Syndromes .
Urticaria Deafness Amyloidosis Syndrome .
Urticaria, Familial Cold .
Urticaria-Deafness-Amyloidosis Syndromes .
Urticarias, Familial Cold .
CINCA Syndrome .
Chronic Infantile Neurological, Cutaneous, and Articular Syndrome .
Cryopyrinopathy .
Familial Cold Autoinflammatory Syndrome .
Familial Cold Urticaria .
IOMID .
Infantile Onset Multisystem Inflammatory Disease .
Muckle-Wells Syndrome .
Multisystem Inflammatory Disease, Neonatal-Onset .
NOMID .
Neonatal Onset Multisystem Inflammatory Disease .
1.00
 
Cri-du-Chat Syndrome .
5p Minus Syndrome .
5p- Syndrome .
Cat Cry Syndrome .
Chromosome 5 Short Arm Deletion Syndrome .
Chromosome 5p Deletion Syndrome .
Crying Cat Syndrome .
Deletion of Short Arm of Chromosome 5 Syndrome .
5p Deletion Syndromes .
5p Minus Syndromes .
5p Syndrome .
5p- Syndrome, Chromosome .
5p- Syndromes .
5p- Syndromes, Chromosome .
Cat Cry Syndromes .
Chromosome 5p- Syndromes .
Cri du Chat Syndrome .
Cri-du-Chat Syndromes .
Crying Cat Syndromes .
Deletion Syndrome, 5p .
Deletion Syndromes, 5p .
Minus Syndrome, 5p .
Minus Syndromes, 5p .
Syndrome, 5p Deletion .
Syndrome, 5p Minus .
Syndrome, 5p- .
Syndrome, Cat Cry .
Syndrome, Chromosome 5p- .
Syndrome, Cri-du-Chat .
Syndrome, Crying Cat .
Syndromes, 5p Deletion .
Syndromes, 5p Minus .
Syndromes, Cat Cry .
Syndromes, Chromosome 5p- .
Syndromes, Cri-du-Chat .
Syndromes, Crying Cat .
Chromosome 5p- Syndrome .
5p Deletion Syndrome .
CRYING CAT SYNDROME .
0.47
 
Syndrome .
Symptom Cluster .
Cluster, Symptom .
Clusters, Symptom .
Symptom Clusters .
Syndromes .
0.44