raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:294049

Reunion Island Larsen-like syndrome

inactive · moved to ORPHA:75496B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome

Synonyms: Multiple joint dislocations-short stature-hyperlaxity-craniofacial dysmorphism syndrome

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enReunion Island Larsen-like syndromeMultiple joint dislocations-short stature-hyperlaxity-craniofacial dysmorphism syndrome
frSyndrome Larsen-like de la RéunionLuxations articulaires multiples-petite taille-hyperlaxité-dysmorphie craniofaciale syndrome
deReunion Insel-Variante des Larsen-SyndromsMultiple Gelenkdislokationen-Kleinwuchs-Gelenkinstabilität-kraniofaziale Dysmorphien-Syndrom
esSíndrome similar a Larsen de la isla de la ReuniónSíndrome de Larsen-like de la isla de la Reunión · Síndrome de múltiples luxaciones articulares-talla baja-hiperlaxitud-dismorfia craneofacial
itSindrome di Larsen dell'Isola di RéunionRLS · Sindrome dislocazioni articolari multiple-bassa statura-iperlassità-dismorfismi craniofacciali
nlLarsen-achtig syndroom van RéunionMultipele gewrichtsluxaties - kleine gestalte - hyperlaxiteit - craniofaciale dysmorfie-syndroom
ptSíndrome Larsen da ilha da Reunião
plZespół Larsena wyspy ReunionRLS · Zespół mnogich przemieszczeń stawów, niskiego wzrostu, nadmiernej luźności w stawach i dysmorfii czaszkowo-twarzowej
csLarsenův syndrom z ostrova ReunionRLS · Syndrom zahrnující mnohočetné dislokace kloubů, hyperlaxitu a kraniofaciální dysmorfismus
ukЛарсен-подібний синдром з острова РеюньйонСиндром множинних вивихів суглобів - низькорослості - гіперлабільності - черепно-лицевого дисморфізму
zh留尼汪岛Larsen样综合征多发性关节脱位-身材矮小-颅面畸形综合征
trReunion Adası Larsen-benzeri sendromÇoklu eklem çıkıkları-kısa boy-hiperlaksite-kraniyofasiyal dismorfizm sendromu

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

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Genes

0 direct

Orphanet records no gene directly on this code.

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Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

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Sources for this card