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English
hyperpigmentation of eyelid
Human disease
dyspigmentation of eyelid
HYPERPIGMENTATION OF EYELIDS
In more languages
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Statements
instance of
class of disease
0 references
subclass of
pigmentation disorder
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:10122
eyelid disease
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:10122
health specialty
neurology
0 references
anatomical location
eyelid
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:10122
on focus list of Wikimedia project
WikiProject Medicine
0 references
ICD-9-CM
374.52
2 references
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:10122
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0007769
exact match
http://purl.obolibrary.org/obo/DOID_10122
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:10122
http://identifiers.org/doid/DOID:10122
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
http://purl.obolibrary.org/obo/HP_0007406
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0007406
Identifiers
MeSH descriptor ID
C562400
mapping relation type
exact match
1 reference
Mondo ID
MONDO_0007769
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
C562400
2 references
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:10122
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0007406
Disease Ontology ID
DOID:10122
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:10122
Experimental Factor Ontology ID
1000711
1 reference
based on heuristic
inferred by common MONDO mappings on source and on Wikidata
Human Phenotype Ontology ID
HP:0007406
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0007406
ICD-10-CM
H02.71
2 references
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:10122
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0007769
Mondo ID
MONDO_0007769
0 references
OMIM ID
145100
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:10122
UMLS CUI
C0155211
2 references
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:10122
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0007406
C4280440
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0007406
C0854438
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0007406
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Wikibooks
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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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