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Mondo Disease Ontology
| Preferred Name | striatonigral degeneration | |
| Synonyms | ||
| Definitions |
A progressive neurodegenerative disorder caused by a disruption in the connection between the striatum and the substantia nigra. It is a type of multiple system atrophy (MSA). Signs and symptoms include rigidity, instability, impaired speech, and slow movements. |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0003122 |
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| database_cross_reference |
UMLS:C0270733 ICD10CM:G23.2 icd11.foundation:195535779 DOID:4751 NCIT:C125695 SCTID:29618004 MEDGEN:124366 MESH:D020955 OMIMPS:271930 ICD9:333.0
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|
| definition |
A progressive neurodegenerative disorder caused by a disruption in the connection between the striatum and the substantia nigra. It is a type of multiple system atrophy (MSA). Signs and symptoms include rigidity, instability, impaired speech, and slow movements.
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|
| id |
MONDO:0003122
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| in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-simple#otar http://purl.obolibrary.org/obo/mondo/mondo-simple#rare |
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| label |
striatonigral degeneration
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| notation |
MONDO:0003122
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| prefLabel |
striatonigral degeneration
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| should_conform_to |
http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml |
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| skos_exactMatch |
http://purl.obolibrary.org/obo/DOID_4751 http://purl.obolibrary.org/obo/NCIT_C125695 http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/195535779 https://omim.org/phenotypicSeries/PS271930 http://identifiers.org/snomedct/29618004 http://identifiers.org/mesh/D020955 http://purl.bioontology.org/ontology/ICD10CM/G23.2 |
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| subClassOf |
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