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(Q55789041)
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English
intestinal malformation
human disease
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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_0019999
class of disease
0 references
subclass of
rare genetic developmental defect during embryogenesis
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0019999
digestive system abnormality
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0019999
intestinal disease
0 references
exact match
http://www.orpha.net/ORDO/Orphanet_97945
0 references
Identifiers
ICD-10
Q43.9
0 references
Medical Dictionary for Regulatory Activities ID
10061067
1 reference
reference URL
https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx
based on heuristic
inferred by common ICD-10 mappings on Wikidata and on source
Mondo ID
MONDO_0019999
0 references
Orphanet ID
97945
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0019999
UMLS CUI
C0745360
0 references
C5681554
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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