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(Q55786577)
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English
partial deletion of chromosome 8
human disease
Partial monosomy of chromosome 8
Partial deletion of chromosome type 8
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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_0016873
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_0016873
exact match
http://www.orpha.net/ORDO/Orphanet_261801
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_0016873
ICD-11 (foundation)
1979614446
0 references
ICD-11 ID (MMS)
LD44.8
subject named as
Deletions of chromosome 8
0 references
Mondo ID
MONDO_0016873
0 references
Orphanet ID
261801
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0016873
UMLS CUI
C5679652
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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