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(Q55788558)
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English
disorder of pyridoxine metabolism
acquired metabolic disease that is has its basis in the disruption of pyridoxine metabolic process
Disorder of pyridoxine metabolism
rare inborn error of pyridoxine metabolic process
inborn error of pyridoxine metabolic process
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Statements
instance of
class of disease
0 references
subclass of
disorder of biogenic amine metabolism and transport
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0019237
vitamin metabolic disorder
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0019237
exact match
http://www.orpha.net/ORDO/Orphanet_79192
0 references
Identifiers
ICD-10-CM
G40.8
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0019237
ICD-11 (foundation)
1860570911
0 references
ICD-11 ID (MMS)
5C59.2
subject named as
Disorders of pyridoxine metabolism
0 references
Mondo ID
MONDO_0019237
0 references
Orphanet ID
79192
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0019237
UMLS CUI
C5681285
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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