raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3323

Braddock-Carey syndrome

inactive · moved to ORPHA:26132321q22.11q22.12 microdeletion syndrome

Synonyms: Thrombocytopenia-Robin sequence 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 21q22.11q22.12 microdeletion syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enBraddock-Carey syndromeThrombocytopenia-Robin sequence syndrome
frSyndrome de Braddock-CareySyndrome de thrombocytopénie-syndrome de Pierre Robin
deThrombozytopenie - Pierre-Robin-SequenzBraddock-Carey-Syndrom
esTrombocitopenia-síndrome de Pierre RobinSíndrome de Braddock-Carey
itTrombocitopenia - sindrome di Pierre RobinSindrome di Braddock-Carey
nlTrombocytopenie - Robin sequentie-syndroomSyndroom van Braddock-Carey
ptSíndrome Braddock-CareySíndrome de trombocitopenia-sequência de Robin
plTrombocytopenia - sekwencja RobinaZespół Braddocka i Carey'a
csSyndrom zahrnující trombocytopenii a Robinovu sekvenciBraddockův-Careyův syndrom · Braddock-Careyův syndrom
ukСиндром Бреддока-КеріСиндром тромбоцитопенії - послідовності Робена
zhBraddock-Carey综合征血小板减少-Robin序列征综合征
trBraddock-Carey sendromuTrombositopeni-Robin dizi sendromu
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