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(Q55786796)
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English
basal encephalocele
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_0017082
class of disease
0 references
subclass of
encephalocele
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017082
exact match
http://www.orpha.net/ORDO/Orphanet_268829
0 references
Identifiers
ICD-10-CM
Q01.8
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017082
ICD-11 (foundation)
533416539
0 references
Mondo ID
MONDO_0017082
0 references
Orphanet ID
268829
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017082
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