ORPHA:180139
Uterine hypoplasia
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare congenital urogenital tract malformation characterized by a small uterus of regular shape (simple uterine hypoplasia), an elongated uterus with normal fundus (elongated uterine hypoplasia), or an abnormally shaped uterus (malformative uterine hypoplasia). Symptoms may include primary amenorrhea, abdominal pain, and infertility.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Uterine hypoplasia | |
| fr | Hypoplasie utérine | |
| de | Uterushypoplasie | |
| es | Hipoplasia uterina | |
| it | Ipoplasia dell'utero | |
| nl | Hypoplasie van uterus | Hypoplasie van baarmoeder · Uteriene hypoplasie |
| pt | Hipoplasia uterina | |
| pl | Hipoplazja macicy | |
| cs | Hypoplázie dělohy | |
| uk | Гіпоплазія матки | |
| zh | 子宫发育不全 | |
| tr | Uterin hipoplazisi |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q51.8 | NTBT | inclusion | validated |
| ICD-11 | LB44.1 | E | specific | validated |
| MONDO | 0015843 | E | validated | |
| UMLS | C0266399 | E | validated | |
| MedDRA | 10063146 | 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:180065Non-syndromic uterovaginal malformation
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare gynecological and obstetric diseases; rare transplant-related disorders
No children.
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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/180139
- This record as JSON: /data/d/180139.json