raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93943

Corpus callosum dysgenesis-hypopituitarism syndrome

inactive · moved to ORPHA:3157Septo-optic dysplasia spectrum

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 Septo-optic dysplasia spectrum

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enCorpus callosum dysgenesis-hypopituitarism syndrome
frSyndrome de dysgénésie du corps calleux-hypopituitarisme
deCorpus-callosum-Dysgenesie mit Hypopituitarismus
esSíndrome de disgenesia del cuerpo calloso-hipopituitarismo
itDisgenesia del corpo calloso - ipopituitarismo
nlDysgenesie van corpus callosum - hypopituïtarisme-syndroom
ptSíndrome de disgenesia do corpo caloso-hipopituitarismo
plDysgenezja ciała modzelowatego - niedoczynność przysadki
csSyndrom zahrnující dysgenezi corpus callosum a hypopituitarismus
ukСиндром дисгенезії мозолистого тіла - гіпопітуїтаризм
zh胼胝体发育不全-垂体功能减退症
trKorpus kallozum disgenezi-hipopituitarizm 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