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hemiparkinsonism-hemiatrophy syndrome
No description defined
HP-HA syndrome
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No label defined
No description defined
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Statements
instance of
class of disease
0 references
subclass of
rare parkinsonian syndrome due to genetic neurodegenerative disease
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017636
exact match
http://www.orpha.net/ORDO/Orphanet_306669
0 references
Identifiers
ICD-10-CM
G20
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017636
ICD-11 ID (Foundation)
193784690
0 references
ICD-11 ID (MMS)
8A00.21
subject named as
Hemiparkinsonism hemiatrophy syndrome
0 references
Mondo ID
MONDO_0017636
0 references
Orphanet ID
306669
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017636
UMLS CUI
C4545231
1 reference
based on heuristic
inferred by common Orphanet mappings on source and on Wikidata
stated in
UMLS 2023
retrieved
16 June 2023
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