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Descriptor English: Hereditary Central Nervous System Demyelinating Diseases
Descriptor Spanish: Enfermedades Desmielinizantes del Sistema Nervioso Central Hereditarias
Descriptor enfermedades desmielinizantes hereditarias del sistema nervioso central
Entry term(s) enfermedades del sistema nervioso central desmielinizantes hereditarias
enfermedades desmielinizantes del sistema nervioso central hereditarias
enfermedades hereditarias del sistema nervioso central desmielinizantes
Scope note: Afecciones hereditarias que se caracterizan por la pérdida de mielina en el sistema nervioso central.
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



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