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(Q56014424)
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English
early-onset nuclear cataract
human disease
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Statements
instance of
class of disease
0 references
subclass of
early-onset partial cataract
0 references
nuclear sclerosis
0 references
exact match
http://purl.obolibrary.org/obo/HP_0011142
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0011142
http://www.orpha.net/ORDO/Orphanet_98991
0 references
Identifiers
MeSH descriptor ID
C563333
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0020376
C563333
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0011142
Human Phenotype Ontology ID
HP:0011142
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0011142
ICD-10-CM
Q12.0
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0020376
Mondo ID
MONDO_0020376
0 references
Orphanet ID
98991
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0020376
UMLS CUI
C0392557
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0020376
C1112705
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0020376
C1832423
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0011142
C5681644
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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