raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1339

OBSOLETE: Cranioacrofacial syndrome

inactive · referred to ORPHA:102285Multiple congenital anomalies/dysmorphic syndrome without intellectual disability

Synonyms: OBSOLETE: Grosse syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Multiple congenital anomalies/dysmorphic syndrome without intellectual disability

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Cranioacrofacial syndromeOBSOLETE: Grosse syndrome
frOBSOLETE : Syndrome cranio-acrofacialOBSOLETE : Syndrome de Grosse
deOBSOLET: Kranio-akro-faziales SyndromOBSOLET: Grosse-Syndrom
esOBSOLETO: Síndrome cráneo-acro-facialOBSOLETO: Síndrome de Grosse
itOBSOLETO: Sindrome cardio-acro-faccialeOBSOLETO: Sindrome di Grosse
nlOBSOLEET: Cranioacrofaciaal syndroomOBSOLEET: Grossesyndroom
ptOBSOLETO: Síndrome cranio-acro-facialOBSOLETO: Síndrome Grosse
plNIEAKTUALNE: Zespól czaszkowo-konczynowo-twarzowyNIEAKTUALNE: Zespół Grosse
csNEAKTUÁLNÍ: Kranioakrofaciální syndrom= en
ukЗАСТАРІЛО: Краніоакрофаціальний синдромЗАСТАРІЛО: Синдром Гросса
zh弃用:颅-肢端-面综合征Grosse综合征
trEski adı: Kranioakrofasiyal sendromuGrosse 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