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(Q27674901)
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English
cataract 7
cataract that has material basis in variation in the region 17q24
CTRCT7
CCA1
Cerulean type cataract 7
congenital Cerulean type cataract 1
cataract type 7
CATARACT 7
CATARACT 7; CTRCT7
Cataract 7, Cerulean Type
Cataract, Congenital, Cerulean Type, 1
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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_0007279
class of disease
0 references
subclass of
cataract
1 reference
stated in
Disease Ontology
retrieved
29 November 2021
Disease Ontology ID
DOID:0110260
autosomal dominant disease
1 reference
stated in
Disease Ontology
retrieved
29 November 2021
Disease Ontology ID
DOID:0110260
health specialty
medical genetics
0 references
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0110260
1 reference
stated in
Disease Ontology
retrieved
29 November 2021
Disease Ontology ID
DOID:0110260
http://identifiers.org/doid/DOID:0110260
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
Identifiers
Disease Ontology ID
DOID:0110260
1 reference
stated in
Disease Ontology
retrieved
29 November 2021
Disease Ontology ID
DOID:0110260
GARD rare disease ID
9508
0 references
ICD-10-CM
Q12.0
2 references
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0110260
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0007279
Mondo ID
MONDO_0007279
0 references
OMIM ID
115660
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0110260
Orphanet ID
217052
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0007279
UMLS CUI
C0344523
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0007279
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