OBSOLETE: Genetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
inactive · referred to ORPHA:611327Genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Synonyms: OBSOLETE: Genetic MCA/variable MR · OBSOLETE: Genetic multiple congenital anomalies-variable intellectual disability with or without dysmorphism syndrome
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Genetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome | OBSOLETE: Genetic MCA/variable MR · OBSOLETE: Genetic multiple congenital anomalies-variable intellectual disability with or without dysmorphism syndrome |
| fr | OBSOLETE : Anomalies congénitales multiples-déficience intellectuelle variable d'origine génétique | OBSOLETE : MCA/MR variable d'origine génétique |
| de | OBSOLET: Genetisch bedingte multiple kongenitale Anomalien/Dysmorphie-Syndrom mit variabler Intelligenzminderung | OBSOLET: Genetisch bedingte multiple kongenitale Anomalien mit variabler Intelligenzminderung · OBSOLET: Genetisch bedingtes multiples Dysmorphie-Syndrom mit variabler Intelligenzminderung |
| es | OBSOLETO: Síndrome de anomalías congénitas múltiples/síndrome dismórfico-discapacidad intelectual variable de origen genético | OBSOLETO: Síndrome de anomalías congénitas múltiples-discapacidad intelectual variable con o sin dismorfia de origen genético |
| it | OBSOLETO: Sindrome genetica da anomalie/dismorfismi congeniti multipli- sindrome disabilità intellettiva variabile | OBSOLETO: Sindrome genetica da anomalie congenite multiple-disabilità intellettiva variabile con o senza dismorfismi · OBSOLETO: MCA/MR variabile, di origine genetica · OBSOLETO: Sindrome genetica da anomalie congenite multiple e disabilità intellettiva variabile con o senza dismorfismi |
| nl | OBSOLEET: Genetische multipele congenitale anomalieën/dysmorfie-syndroom - variabele intellectuele achterstand-syndroom | OBSOLEET: Genetische MCA/variabele MR · OBSOLEET: Genetische multipele congenitale anomalieën - variabele intellectuele achterstand met of zonder dysmorfie-syndroom |
| pt | OBSOLETO: Síndrome de anomalias congénitas múltiplas genéticas/dismorfias-perturbação do desenvolvimento intelectual variável | |
| pl | NIEAKTUALNE: Mnogie genetycznie uwarunkowane wady wrodzone/zespół dysmorficzny-zróżnicowana niepełnosprawność intelektualna | NIEAKTUALNE: Mnogie wady wrodzone uwarunkowane genetycznie - zmienna niepełnosprawność intelektualna z dysmorfią lub bez |
| cs | NEAKTUÁLNÍ: Syndromy zahrnující geneticky podmíněné mnohočetné vrozené vady/dysmorfické syndromy a proměnlivou mentální retardaci | NEAKTUÁLNÍ: Geneticky podmíněné MCA/proměnlivá MR · NEAKTUÁLNÍ: Syndrom zahrnující geneticky podmíněné mnohočetné vrozené vady a proměnlivou mentální retardaci, s nebo bez dysmorfismu |
| uk | ЗАСТАРІЛО: Генетично обумовлені множинні вроджені аномалії/дисморфічний синдром/синдром варіабельної розумової відсталості | ЗАСТАРІЛО: Генетичний MCA/варіабельний МР · ЗАСТАРІЛО: Генетичні множинні вроджені аномалії - варіабельна розумова відсталість із синдромом дисморфізму або без нього |
| zh | 遗传性多发性先天性异常/畸形综合征-多样性智力障碍综合征 | 遗传性MCA/多样性 MR |
| tr | Genetik çoklu doğumsal anomaliler/dismorfik sendrom-değişken zihinsel yetersizlik sendromu | Dismorfizm sendromu olan veya olmayan genetik çoklu doğumsal anomaliler-değişken zihinsel yetersizlik · Genetik MCA / değişken MR |
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
Classification
Not placed in any Orphanet classification in this release.
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/330197
- This record as JSON: /data/d/330197.json