raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1492

OBSOLETE: Corpus callosum agenesis-double urinary collecting system-trigonocephaly syndrome

inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability

Synonyms: OBSOLETE: Ben Ari-Shuper-Mimouni 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-intellectual disability

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Corpus callosum agenesis-double urinary collecting system-trigonocephaly syndromeOBSOLETE: Ben Ari-Shuper-Mimouni syndrome
frOBSOLETE : Syndrome d'agénésie du corps calleux-uretre bifide-trigonocéphalieOBSOLETE : Syndrome de Ben Ari-Shuper-Mimouni
deOBSOLET: Corpus callosum-Agenesie-doppeltes Harnsammelsystem-Trigonozephalus-SyndromOBSOLET: Ben Ari-Shuper-Mimouni-Syndrom
esOBSOLETO: Síndrome de agenesia del cuerpo calloso-doble sistema colector urinario-trigonocefaliaOBSOLETO: Síndrome de Ben Ari-Shuper-Mimouni
itOBSOLETO: Agenesia del corpo calloso-uretra bifida-trigonocefaliaOBSOLETO: Sindrome di Ben Ari-Shuper-Mimouni
nlOBSOLEET: Agenesie van corpus callosum - dubbel urinair verzamelsysteem - trigonocefalie-syndroomOBSOLEET: Syndroom van Ben Ari-Shuper-Mimouni
ptOBSOLETO: Síndrome de agenesia do corpo caloso-duplicação do sistema coletor urinário-trigonocefaliaOBSOLETO: Síndrome Ben-Ari-Shuper-Mimouni
plNIEAKTUALNE: Agnezja ciala modzelowatego - podwójny uklad zbierajacy moczNIEAKTUALNE: Zespół Ben Ari, Shupera i Mimouni
csNEAKTUÁLNÍ: Syndrom zahrnující agenezi corpus callosum a zdvojení sběrného močového systému= en
ukЗАСТАРІЛО: Синдром агенезії мозолистого тіла-подвійної уретри-тригоноцефаліїЗАСТАРІЛО: Синдром Бен Арі-Шупер-Мімуні
zh弃用:胼胝体发育不全-肾盂输尿管重复畸形-三角头畸形综合征Ben Ari-Shuper-Mimouni 综合征
trEski adı: Korpus kallozum agenezi-çift üriner toplama sistemi-trigonosefali sendromuBen Ari-Shuper-Mimouni 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