Preferred Name |
Alexander Disease |
|
Synonyms |
|
|
Definitions |
A rare genetic neurodegenerative disorder which belongs to the group of leukodystrophies. It has a slow and progressive clinical course and is characterized by developmental delay, macrocephaly, seizures, dementia and spasticity. |
|
ID |
http://purl.obolibrary.org/obo/NCIT_C84545 |
|
code |
C84545 |
|
Contributing_Source |
Cellosaurus |
|
definition |
A rare genetic neurodegenerative disorder which belongs to the group of leukodystrophies. It has a slow and progressive clinical course and is characterized by developmental delay, macrocephaly, seizures, dementia and spasticity. |
|
in_subset | ||
label |
Alexander Disease |
|
Preferred_Name |
Alexander Disease |
|
prefixIRI |
NCIT:C84545 |
|
prefLabel |
Alexander Disease |
|
Semantic_Type |
Disease or Syndrome |
|
UMLS_CUI |
C0270726 |
|
subClassOf |
Create mapping