ORPHA:79374
Pigmentation anomaly of the skin
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pigmentation anomaly of the skin | |
| fr | Anomalie de la pigmentation cutanée | |
| de | Pigmentierungsanomalien | |
| es | Anomalía de la pigmentación | |
| it | Anomalie della pigmentazione | |
| nl | Pigmentatie-anomalie van huid | |
| pt | Anomalia da pigmentação cutânea | |
| pl | Zaburzenie pigmentacji skóry | |
| cs | Anomálie kožní pigmentace | |
| uk | Аномалія пігментації шкіри | |
| zh | 皮肤色素沉着异常 | |
| tr | Derinin pigmentasyon anomalisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019288 | E | validated | |
| MONDO | 19288 | E | validated | |
| UMLS | C5681482 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:89826Rare skin disease
rare skin diseases
Children (5):
- ORPHA:280628Familial progressive hyper- and hypopigmentation
- ORPHA:79375Hyperpigmentation of the skin
- ORPHA:2435Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome
- ORPHA:79376Hypopigmentation of the skin
- ORPHA:447961Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome
Codes that Orphanet moved or referred to this one:
- ORPHA:98700OBSOLETE: Pigmentation disorder with eye involvement referred to · inactive
- ORPHA:98708OBSOLETE: Pigmentation disorder with eye involvement, excluding albinism referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/79374
- This record as JSON: /data/d/79374.json