| ADR Ontology |
| ADR Term |
Skin hypopigmentation |
| ADR ID |
BADD_A04043 |
| ADR Hierarchy |
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| Description |
A disorder characterized by loss of skin pigment (e.g., vitiligo). [CTCAE] 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] |
| MedDRA Code |
10040868 |
| MeSH ID |
D017496
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ADR Severity Grade (FAERS)
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ADR Severity Grade (CTCAE)
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| Synonym |
| Skin hypopigmentation | Hypomelanosis | Hypopigmentation | Hypomelanoses |
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| ADR Related Proteins |
| Protein Name |
UniProt AC |
TTD Target ID |
| Not Available | Not Available | Not Available |
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| Drugs Leading to the ADR |
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