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(Q55788263)
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English
pseudohypoparathyroidism with Albright hereditary osteodystrophy
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_0018699
class of disease
0 references
subclass of
other dermis disorder
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0018699
acromelic dysplasia
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0018699
other genetic dermis disorder
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0018699
musculoskeletal disease with cataract
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0018699
syndromic obesity
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0018699
pseudohypoparathyroidism
0 references
exact match
http://www.orpha.net/ORDO/Orphanet_457059
0 references
Identifiers
Mondo ID
MONDO_0018699
0 references
Orphanet ID
457059
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0018699
UMLS CUI
C5681125
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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