hereditary central nervous system demyelinating diseases

Preferred Label : hereditary central nervous system demyelinating diseases;

MeSH definition : Inherited conditions characterized by a loss of MYELIN in the central nervous system.;

MeSH synonym : demyelinating central nervous system diseases, hereditary; hereditary demyelinating diseases, central nervous system; central nervous system demyelinating hereditary diseases; central nervous system hereditary demyelinating diseases; central nervous system demyelinating diseases, hereditary; demyelinating diseases, central nervous system, hereditary;

Details

Origin ID

D020279;

UMLS CUI

C0751877;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Currated CISMeF NLP mapping
- hereditary central nervous system demyelinating disorder [Disease (Nov.)]
Record concept(s)
- hereditary central nervous system demyelinating diseases [MeSH concept]
Related MeSH Supplementary Concept(s)
- dysmyelination with jaundice [MeSH Supplementary Concept]
- hypomyelination, global cerebral [MeSH Supplementary Concept]
- leukodystrophy, dysmyelinating, with oligodontia [MeSH Supplementary Concept]
- leukodystrophy, hypomyelinating, 2 [MeSH Supplementary Concept]
- leukodystrophy, hypomyelinating, 4 [MeSH Supplementary Concept]
- leukodystrophy, hypomyelinating, 5 [MeSH Supplementary Concept]
- leukodystrophy, hypomyelinating, 6 [MeSH Supplementary Concept]
- megalencephalic leukoencephalopathy with subcortical cysts [MeSH Supplementary Concept]
- megalencephaly with dysmyelination [MeSH Supplementary Concept]
- optic atrophy with demyelinating disease of CNS [MeSH Supplementary Concept]
- vasculopathy, retinal, with cerebral leukodystrophy [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- hereditary central nervous system demyelinating disorder [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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