ORPHA:696897
Congenital megaprepuce
Synonyms: Isolated congenital buried penis
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Multigenic/multifactorial
- Age of onset
- Neonatal
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital megaprepuce | Isolated congenital buried penis |
| fr | Méga-prépuce congénital | Verge enfouie congénitale |
| de | Megapräputium, kongenitales | Isolierter kongenitaler Buried-Penis |
| es | Megaprepucio congénito | Pene enterrado congénito aislado |
| it | Megaprepuzio congenito | Pene infossato congenito isolato |
| nl | Congenitaal megapreputium | Geïsoleerde congenitale begraven penis |
| pt | Congenital Megaprepuce | |
| pl | Congenital megaprepuce | = en |
| cs | Congenital megaprepuce | = en |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q55.6 | NTBT | attributed | 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:182121Non-syndromic urogenital tract malformation of male
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare transplant-related disorders
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 868 cases | Worldwide | Case(s) | Validated | ORPHANET | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/696897
- This record as JSON: /data/d/696897.json