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7p22.1 microduplication syndrome
No description defined
Dup(7)(p22.1)
Trisomy 7p22.1
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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_0017792
class of disease
0 references
subclass of
multiple congenital anomalies/dysmorphic syndrome-intellectual disability
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017792
partial duplication of the short arm of chromosome 7
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017792
genetic syndromic intellectual disability
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017792
exact match
http://www.orpha.net/ORDO/Orphanet_314034
0 references
Identifiers
ICD-10-CM
Q92.3
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017792
Mondo ID
MONDO_0017792
0 references
Orphanet ID
314034
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017792
UMLS CUI
C4707093
1 reference
based on heuristic
inferred by common Orphanet mappings on source and on Wikidata
stated in
UMLS 2023
retrieved
16 June 2023
WikiProjectMed ID
7p22.1 microduplication syndrome
0 references
Sitelinks
Wikipedia
(1 entry)
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enwiki
7p22.1 microduplication syndrome
Wikibooks
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Wikinews
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Wikiversity
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Wikivoyage
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Wiktionary
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Multilingual sites
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