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(Q55781373)
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English
robin sequence-oligodactyly syndrome
human disease
Pierre Robin sequence-oligodactyly syndrome
PIERRE ROBIN SYNDROME AND OLIGODACTYLY
Robin Sequence and Oligodactyly
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No label defined
No description defined
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Statements
instance of
head and neck disease
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008247
developmental defect during embryogenesis
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008247
class of disease
0 references
subclass of
orofacial clefting syndrome
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008247
Pierre Robin syndrome
0 references
exact match
http://www.orpha.net/ORDO/Orphanet_3104
0 references
Identifiers
MeSH descriptor ID
C535688
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008247
ICD-10-CM
Q87.0
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008247
Mondo ID
MONDO_0008247
0 references
OMIM ID
172880
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008247
Orphanet ID
3104
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008247
UMLS CUI
C1868309
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008247
C4749398
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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