ORPHA:180193
Syndromic breast hypoplasia/aplasia
- 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 breast hypoplasia/aplasia | |
| fr | Hypoplasie/aplasie mammaire syndromique | |
| de | Mammaaplasie, syndromale | |
| es | Hipoplasia/aplasia mamaria sindrómica | |
| it | Aplasia/ipoplasia mammaria sindromica | |
| nl | Syndromale borsthypoplasie/aplasie | |
| pt | Aplasia mamária sindromática | |
| pl | Syndromiczna hipoplazja/aplazja piersi | |
| cs | Syndromická hypoplázie/aplázie prsní žlázy | |
| uk | Синдромальна гіпоплазія/аплазія молочних залоз | |
| zh | 综合征性乳房发育不全/未发育 | |
| tr | Sendromik meme hipoplazisi / aplazisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015856 | E | validated | |
| MONDO | 15856 | E | validated | |
| UMLS | C5680482 | 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:180173Deficient breast volume or number
rare gynecological and obstetric diseases
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/180193
- This record as JSON: /data/d/180193.json