loading...| Preferred Name | primary cerebellar degeneration | |
| Synonyms | ||
| Definitions |
A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked. |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0004742 |
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| database_cross_reference |
ICD9:334.2 SCTID:23732000 UMLS:C0033132 DOID:9277 MEDGEN:19466 |
|
| definition |
A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked. |
|
| id |
MONDO:0004742 |
|
| label |
primary cerebellar degeneration |
|
| notation |
MONDO:0004742 |
|
| prefLabel |
primary cerebellar degeneration |
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| skos_exactMatch |
http://purl.obolibrary.org/obo/DOID_9277 http://identifiers.org/medgen/19466 |
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| treeView | ||
| subClassOf |