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(Q55786982)
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English
disorders of vitamin D metabolism
human disease
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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_0017322
class of disease
0 references
subclass of
rare parathyroid disease and phosphocalcic metabolism anomaly
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017322
primary bone dysplasia with defective bone mineralization
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017322
rare genetic parathyroid disease and phosphocalcic metabolism disorder
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017322
vitamin metabolic disorder
0 references
exact match
http://www.orpha.net/ORDO/Orphanet_289098
0 references
Identifiers
Mondo ID
MONDO_0017322
0 references
Orphanet ID
289098
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0017322
UMLS CUI
C5681017
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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