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(Q55785653)
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English
familial scaphocephaly syndrome
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_0015704
class of disease
0 references
subclass of
syndromic craniosynostosis
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0015704
exact match
http://www.orpha.net/ORDO/Orphanet_169163
0 references
Identifiers
ICD-10-CM
Q75.0
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0015704
Mondo ID
MONDO_0015704
0 references
Orphanet ID
169163
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0015704
UMLS CUI
C3267076
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0015704
UniProt disease ID
DI-00498
0 references
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Wikisource
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Wikiversity
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Multilingual sites
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