raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2352

Kozlowski-Brown-Hardwick syndrome

inactive · moved to ORPHA:2462Shprintzen-Goldberg 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 Shprintzen-Goldberg syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enKozlowski-Brown-Hardwick syndrome
frSyndrome de Kozlowski-Brown-Hardwick
deKozlowski-Brown-Hardwick-Syndrom
esSíndrome de Kozlowski-Brown-Hardwick
itSindrome di Kozlowski-Brown-Hardwick
nlSyndroom van Kozlowski-Brown-Hardwick
ptSíndrome Kozlowski-Brown-Hardwick
plZespół Kozłowskiego, Browna i Hardwicka
csKozlowského-Brownův-Hardwickův syndromKozlowski-Brown-Hardwickův syndrom
ukСиндром Козловського-Брауна-Хардвіка
zhKozlowski-Brown-Hardwick 综合征
trKozlowski-Brown-Hardwick sendromu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MeSHC537506Evalidated
UMLSC2931511Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

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