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(Q54931797)
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English
mouth abnormality
congenital absence of or defects in structures of the mouth
mouth abnormalities
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Statements
instance of
disease
0 references
subclass of
mouth disease
0 references
craniofacial abnormality
0 references
stomatognathic system abnormality
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health specialty
oral and maxillofacial surgery
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exact match
http://purl.obolibrary.org/obo/HP_0000153
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000153
topic's main category
Category:Congenital oral disorders
0 references
Identifiers
National Library of Latvia ID
000320249
0 references
MeSH descriptor ID
D009056
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000153
MeSH tree code
C07.465.525
0 references
C07.650.525
0 references
C16.131.850.525
0 references
Human Phenotype Ontology ID
HP:0000153
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000153
ICD-10
Q38.6
0 references
Medical Dictionary for Regulatory Activities ID
10061070
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
UMLS CUI
C0026633
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000153
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