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choroid disease
human disease
Choroid disorder
Choroid disorder NOS (disorder)
Choroidal disorder
Unspecified disorder of choroid
choroid disorder
disorder of optic choroid
disease of optic choroid
choroid diseases
In more languages
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Statements
instance of
class of disease
0 references
subclass of
uveal disease
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:1417
health specialty
neurology
0 references
anatomical location
choroid
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:1417
on focus list of Wikimedia project
WikiProject Medicine
0 references
ICD-9-CM
363.9
2 references
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:1417
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
27 July 2018
Mondo ID
MONDO_0001898
363.8
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
27 July 2018
Mondo ID
MONDO_0001898
NCI Thesaurus ID
C34468
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:1417
exact match
http://purl.obolibrary.org/obo/DOID_1417
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:1417
http://identifiers.org/doid/DOID:1417
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
http://purl.obolibrary.org/obo/HP_0000610
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000610
Identifiers
NL CR AUT ID
ph1030152
subject named as
nemoci cévnatky
0 references
MeSH descriptor ID
D015862
mapping relation type
exact match
subject named as
Choroid Diseases
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
27 July 2018
Mondo ID
MONDO_0001898
MeSH tree code
C11.941.160
0 references
Disease Ontology ID
DOID:1417
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:1417
Human Phenotype Ontology ID
HP:0000610
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000610
ICD-10-CM
H31.9
2 references
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:1417
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
27 July 2018
Mondo ID
MONDO_0001898
ICD-11 (foundation)
146528463
0 references
Mondo ID
MONDO_0001898
0 references
UMLS CUI
C0008521
2 references
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:1417
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000610
C4025836
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000610
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Wikinews
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Wikiquote
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Wikisource
(0 entries)
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Wikiversity
(0 entries)
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Wikivoyage
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Wiktionary
(0 entries)
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Multilingual sites
(0 entries)
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