ORPHA:79370
Syndromic nail anomaly
- 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 | Syndromic nail anomaly | |
| fr | Anomalie syndromique des ongles | |
| de | Nagelkrankheit, syndromale | |
| es | Trastorno sindrómico de las uñas | |
| it | Anomalie sindromiche delle unghie | |
| nl | Syndromale nagelanomalie | |
| pt | Anomalia sindromática das unhas | |
| pl | Syndromiczna wada paznokci | |
| cs | Syndromické anomálie nehtů | |
| uk | Синдромальна аномалія нігтів | |
| zh | 综合征性甲异常 | |
| tr | Sendromik tırnak anomalisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19285 | E | validated | |
| UMLS | C5681480 | 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 (2):
- ORPHA:183454Genetic nail anomaly
rare genetic diseases - ORPHA:79368Nail anomaly
rare skin diseases
Children (16):
- ORPHA:4958189q33.3q34.11 microdeletion syndrome
- ORPHA:69125Anonychia with flexural pigmentation
- ORPHA:1487Cooks syndrome
- ORPHA:3231Deafness-onychodystrophy syndrome
- ORPHA:2045FLOTCH syndrome
- ORPHA:2153Hirschsprung disease-nail hypoplasia-dysmorphism syndrome
- ORPHA:330029Hypotrichosis-deafness syndrome
- ORPHA:210133Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome
- ORPHA:662Lymphedema with yellow nails
- ORPHA:2614Nail-patella syndrome
- ORPHA:1811Odontomicronychial dysplasia
- ORPHA:2793Otoonychoperoneal syndrome
- ORPHA:2309Pachyonychia congenita
- ORPHA:2835Pectus excavatum-macrocephaly-dysplastic nails syndrome
- ORPHA:488232Split-foot malformation-mesoaxial polydactyly syndrome
- ORPHA:420561Temple-Baraitser syndrome
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/79370
- This record as JSON: /data/d/79370.json