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English
Axenfeld-Rieger syndrome type 2
Axenfeld-Rieger syndrome that has material basis in deletions in the region 13q14
RIEG2
Rieger syndrome type 2
AXENFELD-RIEGER SYNDROME, TYPE 2
AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2
Rieger Syndrome, Type 2
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Statements
instance of
class of disease
0 references
subclass of
Axenfeld-Rieger syndrome
1 reference
stated in
Disease Ontology
retrieved
18 January 2022
Disease Ontology ID
DOID:0110121
chromosomal deletion syndrome
1 reference
stated in
Disease Ontology
retrieved
18 January 2022
Disease Ontology ID
DOID:0110121
health specialty
medical genetics
0 references
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0110121
1 reference
stated in
Disease Ontology
retrieved
18 January 2022
Disease Ontology ID
DOID:0110121
http://identifiers.org/doid/DOID:0110121
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
Identifiers
MeSH descriptor ID
C535680
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
6 August 2018
Mondo ID
MONDO_0011097
Disease Ontology ID
DOID:0110121
1 reference
stated in
Disease Ontology
retrieved
18 January 2022
Disease Ontology ID
DOID:0110121
ICD-10-CM
Q13.8
2 references
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0110121
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
6 August 2018
Mondo ID
MONDO_0011097
Mondo ID
MONDO_0011097
0 references
OMIM ID
601499
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0110121
601499
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
6 August 2018
Mondo ID
MONDO_0011097
UMLS CUI
C1832229
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
6 August 2018
Mondo ID
MONDO_0011097
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Wikiversity
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Multilingual sites
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