raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2243

Hypopituitarism-micropenis-cleft lip/palate 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
enHypopituitarism-micropenis-cleft lip/palate syndrome
frSyndrome d'hypopituitarisme-micropénis-fente labiopalatine
deHypopituitarismus - Mikropenis - Lippen-Kiefer-Gaumenspalte
esSíndrome de hipopituitarismo-micropene-fisura labiopalatina
itIpopituitarismo - micropene - labiopalatoschisi
nlHypopituïtarisme - micropenis - gespleten lip/gehemelte-syndroom
ptSíndrome de hipopituitarismo-micropénis-fenda lábio-palatina
plNiedoczynność przysadki - mikropenis - rozszczep wargi/podniebienia
csSyndrom zahrnující hypopituitarismus, mikropenis a rozštěp rtu a patra
ukСиндром гіпопітуїтаризму-мікропеніса-розщілини губи/піднебіння
zh垂体机能减退-小阴茎-唇/腭裂综合征
trHipopituitarizm-mikropenis-yarık dudak / damak 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