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loading...| Preferred Name | Hypopigmentation [Disease/Finding] | |
| Synonyms |
Hypopigmentation Hypomelanosis |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000003588 |
|
| altLabel |
Hypopigmentation Hypomelanosis |
|
| cui |
C0162835 |
|
| May be treated by | ||
| 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 name |
Hypopigmentation |
|
| MESH UI |
M0026547 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000003588 |
|
| NUI |
N0000003588 |
|
| prefLabel |
Hypopigmentation [Disease/Finding] |
|
| SNOMED CID |
201284005 23006000 |
|
| tui |
T047 |
|
| subClassOf |
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