ORPHA:964
Acromegaly-cutis verticis gyrata-corneal leukoma syndrome
inactive · moved to ORPHA:2796Pachydermoperiostosis
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Pachydermoperiostosis
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acromegaly-cutis verticis gyrata-corneal leukoma syndrome | |
| fr | Syndrome d'acromégalie-cutis verticis gyrata-leucome cornéen | |
| de | Akromegalie-Cutis verticis gyrata-Kornea-Leukom-Syndrom | |
| es | Síndrome de acromegalia-cutis verticis gyrata-leucoma corneal | |
| it | Sindrome acromegalia-cutis verticis gyrata-leucoma corneale | |
| nl | Acromegalie - cutis verticis gyrata - corneaal leukoom-syndroom | |
| pt | Síndrome de acromegalia-cutis verticis gyrata-leucoma da córnea | |
| pl | Zespół akromegalii, skóry krętej ciemienej i bielma rogówki | |
| cs | Syndrom zahrnující akromegalii, cutis verticis gyrata a korneální leukom | |
| uk | Синдром акромегалії-складчастої пахідермії-лейкоми рогівки | |
| zh | 肢端肥大-回状颅皮-角膜白斑综合征 | |
| tr | Akromegali cutis verdis gyrata -korneal lökoma sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 102100 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
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/964
- This record as JSON: /data/d/964.json