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(Q55789084)
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English
total autosomal monosomy
human disease
In more languages
default values for all languages
No label defined
No description defined
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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_0020053
class of disease
0 references
subclass of
autosomal monosomy
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0020053
exact match
http://www.orpha.net/ORDO/Orphanet_98141
0 references
Identifiers
ICD-10-CM
Q93.0
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0020053
Q93.1
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0020053
ICD-11 ID (Foundation)
599695253
0 references
595685802
0 references
ICD-11 ID (MMS)
LD43.0
subject named as
Complete monosomy of autosome
0 references
Mondo ID
MONDO_0020053
0 references
Orphanet ID
98141
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0020053
UMLS CUI
C5681502
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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