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Descritor em português: | Doenças Desmielinizantes Hereditárias do Sistema Nervoso Central | ||||||
Descritor em inglês: | Hereditary Central Nervous System Demyelinating Diseases | ||||||
Descritor em espanhol: |
Enfermedades Desmielinizantes del Sistema Nervioso Central Hereditarias
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Descritor em francês: | Maladies démyélinisantes héréditaires du système nerveux central | ||||||
Termo(s) alternativo(s): |
Central Nervous System Demyelinating Diseases, Hereditary Central Nervous System Demyelinating Hereditary Diseases Central Nervous System Hereditary Demyelinating Diseases Demyelinating Central Nervous System Diseases, Hereditary Demyelinating Diseases, Central Nervous System, Hereditary Hereditary Demyelinating Diseases, Central Nervous System |
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Código(s) hierárquico(s): |
C10.228.140.163.100.362 C10.228.140.695.625 C10.314.400 C10.574.500.490 C16.320.400.367 C16.320.565.189.362 C18.452.132.100.362 C18.452.648.189.362 |
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Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D020279 | ||||||
Nota de escopo: | Inherited conditions characterized by a loss of MYELIN in the central nervous system. |
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Qualificadores permitidos: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Nota MeSH pública: | 2000 |
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Nota histórica: | 2000 |
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Versão alternativa: | HEREDITARY CNS DEMYELINATING DIS |
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Identificador DeCS: | 34309 | ||||||
ID do descritor: | D020279 | ||||||
Documentos indexados na Biblioteca Virtual em Saúde (BVS): | Clique aqui para acessar os documentos da BVS | ||||||
Data de estabelecimento: | 01/01/2000 | ||||||
Data de entrada: | 03/11/1999 | ||||||
Data de revisão: | 30/06/2018 |
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Hereditary Central Nervous System Demyelinating Diseases
- Conceito preferido
Identificador do conceito |
M0328329 |
Nota de escopo | Inherited conditions characterized by a loss of MYELIN in the central nervous system. |
Termo preferido | Hereditary Central Nervous System Demyelinating Diseases |
Termo(s) alternativo(s) |
Central Nervous System Demyelinating Diseases, Hereditary Central Nervous System Demyelinating Hereditary Diseases Central Nervous System Hereditary Demyelinating Diseases Demyelinating Central Nervous System Diseases, Hereditary Demyelinating Diseases, Central Nervous System, Hereditary Hereditary Demyelinating Diseases, Central Nervous System |
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