raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1266

Dermato-cardio-skeletal syndrome, Borrone type

inactive · moved to ORPHA:137834Frank-Ter Haar 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 Frank-Ter Haar syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enDermato-cardio-skeletal syndrome, Borrone type
frSyndrome dermato-cardio-squelettique type Borrone
deDermato-kardio-skelettales Syndrom Typ Borrone
esSíndrome dermo-cardio-esquelético tipo BorroneSíndrome cutáneo-cardio-osteoarticular, tipo Borrone
itSindrome dermo-cardio-scheletrica, tipo Borrone
nlDermato-cardio-skeletaal syndroom, Borrone-type
ptSíndrome dermato-cardio-esquelético, tipo Boronne
plZespół skórno-sercowo-szkieletowy typu Borrone'a
csDermatokardioskeletální syndrom, Borroneův typ
ukДермато-кардіо-скелетний синдром, тип Борроне
zh皮肤-心脏-骨骼综合征,Borrone 型
trDermato-kardiyo-iskelet sendromu, Borrone tipi
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.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

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.

7

Sources for this card