loading...| Preferred Name |
obsolete_Alexander disease |
|
| Synonyms |
AxD |
|
| Definitions |
Alexander disease (AxD) is a rare neurodegenerative disorder of the astrocytes comprised of two clinical forms: AxD Type I and Type II (see these terms) manifesting with various degrees of macrocephaly, spasticity, ataxia and seizures and leading to psychomotor regression and death. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_58 |
|
| Obsolete |
true |
|
| database_cross_reference |
UMLS:C0270726 MedDRA:10083059 MeSH:D038261 ICD10:E75.2 OMIM:203450 |
|
| definition |
Alexander disease (AxD) is a rare neurodegenerative disorder of the astrocytes comprised of two clinical forms: AxD Type I and Type II (see these terms) manifesting with various degrees of macrocephaly, spasticity, ataxia and seizures and leading to psychomotor regression and death. |
|
| definition_citation |
orphanet |
|
| deprecated |
true |
|
| has_exact_synonym |
AxD |
|
| label |
obsolete_Alexander disease |
|
| obsoleted_in_version |
3.41.0 |
|
| prefLabel |
obsolete_Alexander disease |
|
| reason_for_obsolescence |
Replaced with Mondo term. |
|
| term replaced by | ||
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://www.orpha.net/ORDO/Orphanet_58 | ORDO | SAME_URI |