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(Q2565692)
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English
abrachia
birth defect
Abrachie
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Statements
instance of
concept
0 references
genetic disease
0 references
developmental defect during embryogenesis
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017437
class of disease
0 references
subclass of
amelia
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017437
reduction defects of upper limb
0 references
part of
veterinary medicine
0 references
health specialty
medical genetics
0 references
described by source
Ottův slovník naučný
statement is subject of
Q23848890
1 reference
inferred from
Q23848890
exact match
http://purl.obolibrary.org/obo/HP_0009812
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0009812
http://www.orpha.net/ORDO/Orphanet_294967
0 references
Identifiers
Den Store Danske ID
abrachi
0 references
Freebase ID
/m/0gcyjc
1 reference
stated in
Freebase Data Dumps
publication date
28 October 2013
Human Phenotype Ontology ID
HP:0009812
2 references
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017437
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0009812
ICD-10
Q73.0
1 reference
imported from Wikimedia project
English Wikipedia
ICD-10-CM
Q71.0
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017437
ICD-11 (foundation)
565435388
0 references
ICD-11 ID (MMS)
LB99.0
subject named as
Amelia of upper limb
0 references
ICD-9 ID
755.21
1 reference
imported from Wikimedia project
English Wikipedia
755.31
1 reference
imported from Wikimedia project
English Wikipedia
755.4
1 reference
imported from Wikimedia project
English Wikipedia
Medical Dictionary for Regulatory Activities ID
10000336
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_0017437
0 references
Orphanet ID
294967
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017437
UMLS CUI
C4024200
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0009812
Sitelinks
Wikipedia
(3 entries)
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dawiki
Abrachi
dewiki
Abrachie
plwiki
Abrachia
Wikibooks
(0 entries)
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Wikinews
(0 entries)
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Wikiquote
(0 entries)
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Wikisource
(0 entries)
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Wikiversity
(0 entries)
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Wikivoyage
(0 entries)
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Wiktionary
(0 entries)
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Multilingual sites
(0 entries)
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