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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
| Id | http://purl.bioontology.org/ontology/NDFRT/N0000003588
http://purl.bioontology.org/ontology/NDFRT/N0000003588
|
|---|---|
| Preferred Name | Hypopigmentation [Disease/Finding] |
| Synonyms |
Hypopigmentation
Hypomelanosis
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Hypopigmentation
Hypomelanosis
|
|---|---|
| prefLabel | Hypopigmentation [Disease/Finding]
|
| MESH DEFINITION | A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized or generalized, and may result from genetic defects, trauma, inflammation, or infections.
|
| MESH DUI | D017496
|
| MESH UI | M0026547
|
| MeSH name | Hypopigmentation
|
| type | |
| tui | T047
|
| SNOMED CID |
201284005
23006000
|
| May be treated by | |
| notation | N0000003588
|
| Semantic type UMLS property | |
| NUI | N0000003588
|
| cui | C0162835
|
| NDFRT kind | DISEASE_KIND
|
| subClassOf |
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |