ORPHA:99142
Microcephaly-cutis verticis gyrata-lymphedema syndrome
inactive · moved to ORPHA:193Cohen syndrome
- 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 Cohen syndrome
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Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Microcephaly-cutis verticis gyrata-lymphedema syndrome | |
| fr | Syndrome de microcéphalie-cutis verticis gyrata-lymphoedème | |
| de | Mizrocephalie - Cutis verticis gyrata - Lymphödem | |
| es | Síndrome de microcefalia-cutis verticis gyrata-linfedema | |
| it | Microcefalia - cutis verticis gyrata - linfedema | |
| nl | Microcefalie - cutis verticis gyrata - lymfoedeem | |
| pt | Síndrome de microcefalia-cutis verticis gyrata-linfedema | |
| pl | Mikrocefalia - skóra kręta ciemienia - obrzęk limfatyczny | |
| cs | Syndrom zahrnující mikrocefalii, cutis verticis gyrata a lymfedém | |
| uk | Синдром мікроцефалії-складчастої пахідермії (cutis vertigus gypata)- лімфедеми |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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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/99142
- This record as JSON: /data/d/99142.json