| Descriptor English: | Hereditary Central Nervous System Demyelinating Diseases | ||||||
| Descriptor Spanish: |
Enfermedades Desmielinizantes del Sistema Nervioso Central Hereditarias
| ||||||
| Descriptor Portuguese: | Doenças Desmielinizantes Hereditárias do Sistema Nervoso Central | ||||||
| Descriptor French: | Maladies démyélinisantes héréditaires du système nerveux central | ||||||
| Entry term(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 |
||||||
| Tree number(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 |
||||||
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D020279 | ||||||
| Scope note: | Inherited conditions characterized by a loss of MYELIN in the central nervous system. |
||||||
| Allowable Qualifiers: |
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 |
||||||
| Public MeSH Note: | 2000 |
||||||
| History Note: | 2000 |
||||||
| Entry Version: | HEREDITARY CNS DEMYELINATING DIS |
||||||
| DeCS ID: | 34309 | ||||||
| Unique ID: | D020279 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2000/01/01 | ||||||
| Date of Entry: | 1999/11/03 | ||||||
| Revision Date: | 2018/06/30 |
|
|
Hereditary Central Nervous System Demyelinating Diseases
- Preferred
| Concept UI |
M0328329 |
| Scope note | Inherited conditions characterized by a loss of MYELIN in the central nervous system. |
| Preferred term | Hereditary Central Nervous System Demyelinating Diseases |
| Entry term(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 |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
