ORPHA:98609
EEC syndrome and related disorders
Synonyms: EEC syndrome and related syndrome · Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome and related disorders
- 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 | EEC syndrome and related disorders | EEC syndrome and related syndrome · Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome and related disorders |
| fr | Syndrome EEC et maladies associées | Syndrome d'ectrodactylie-dysplasie ectodermique-fente labiopalatine et maladies associées |
| de | EEC-Syndrom und verwandte Störungen | EEC-Syndrom und verwandte Syndrome · Ektrodaktylie-ektodermale Dysplasie-Lippen-Kiefer-Gaumen-Syndrom und verwandte Störungen |
| es | Síndrome EEC y trastornos relacionados | Síndrome EEC y síndromes relacionados · Síndrome de ectrodactilia-displasia ectodérmica-labio/paladar hendido y trastornos relacionados |
| it | Sindrome EEC e malattie correlate | Sindrome EEC e sindrome correlata · Sindrome ectrodattilia, displasia ectodermica, labio/palatoschisi e malattie correlate |
| nl | EEC-syndroom en gerelateerde aandoeningen | EEC-syndroom en gerelateerd syndroom · Ectrodactylie - ectodermal dysplasie - gespleten lip/verhemelte-syndroom en gerelateerde aandoeningen |
| pt | Síndrome EEC e doenças relacionadas | |
| pl | Zespół EEC i zaburzenia pokrewne | = en |
| cs | Syndrom EEC a příbuzné syndromy | = en |
| uk | Синдром EEC та повязані з ним розлади | Синдром ектродактилії - ектодермальної дисплазії - розщілини губи/піднебіння та повязані з ним розлади · Синдром EEC та повязані з ним синдроми |
| zh | EEC综合征及其相关性疾病 | EEC综合征及其相关综合征 |
| tr | EEC sendromu ve ilgili bozukluklar | EEC sendromu ve ilgili sendrom |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680323 | 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 (3):
- ORPHA:79373Ectodermal dysplasia syndrome
rare developmental anomalies during embryogenesis; rare genetic diseases; rare skin diseases - ORPHA:98602Rare disorder of the lacrimal apparatus
rare ophthalmic disorders - ORPHA:522532Rare genetic disorder of the lacrimal apparatus
rare genetic 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/98609
- This record as JSON: /data/d/98609.json