ORPHA:79376
Hypopigmentation 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hypopigmentation of the skin | |
| fr | Hypopigmentation cutanée | |
| de | Hypopigmentierung | |
| es | Hipopigmentación | |
| it | Ipopigmentazione | |
| nl | Hypopigmentatie van huid | |
| pt | Hipopigmentação cutânea | |
| pl | Hipopigmentacja skóry | |
| cs | Hypopigmentace kůže | |
| uk | Гіпопігментація шкіри | |
| zh | 皮肤色素沉着过少 | |
| tr | Derinin hipopigmentasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019290 | E | validated | |
| MONDO | 19290 | E | validated | |
| MeSH | D017496 | E | validated | |
| UMLS | C0162835 | E | validated | |
| MedDRA | 10040868 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:79374Pigmentation anomaly of the skin
rare skin diseases
Children (14):
- ORPHA:998Albinism-deafness syndrome
- ORPHA:726452Combined immunodeficiency with early gray hairing
- ORPHA:3214Deaf blind hypopigmentation syndrome, Yemenite type
- ORPHA:717846Developmental delay-facial dysmorphism-Blaschko lines hypopigmentation-obesity-intellectual disability syndrome
- ORPHA:589608Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
- ORPHA:55Oculocutaneous albinism
- ORPHA:163746Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease
- ORPHA:2885Piebald trait-neurologic defects syndrome
- ORPHA:2884Piebaldism
- ORPHA:284811Syndromic oculocutaneous albinism
- ORPHA:42665Tietz syndrome
- ORPHA:1493Vici syndrome
- ORPHA:3440Waardenburg syndrome
- ORPHA:897Waardenburg-Shah syndrome
Codes that Orphanet moved or referred to this one:
- ORPHA:435OBSOLETE: Ito hypomelanosis 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.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/79376
- This record as JSON: /data/d/79376.json