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(Q55786629)
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English
partial deletion of the long arm of chromosome 22
human disease
Partial deletion of chromosome 22q
Partial deletion of the long arm of chromosome type 22
Partial monosomy of chromosome 22q
Partial monosomy of the long arm of chromosome 22
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Statements
instance of
developmental defect during embryogenesis
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0016920
class of disease
0 references
subclass of
partial autosomal monosomy
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0016920
exact match
http://www.orpha.net/ORDO/Orphanet_262182
0 references
Identifiers
ICD-10-CM
Q93.5
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0016920
ICD-11 (foundation)
1794672824
0 references
ICD-11 ID (MMS)
LD44.N
subject named as
Deletions of chromosome 22
0 references
Mondo ID
MONDO_0016920
0 references
Orphanet ID
262182
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0016920
UMLS CUI
C5679725
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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