raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2244

Hypopituitarism-microphthalmia syndrome

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

Synonyms: Kaplowitz-Bodurtha syndrome

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-microphthalmia syndromeKaplowitz-Bodurtha syndrome
frSyndrome d'hypopituitarisme-microphtalmieSyndrome de Kaplowitz-Bodurtha
deHypopituitarismus - MikrophthalmieKaplowitz-Bodurtha-Syndrom
esSíndrome de hipopituitarismo-microftalmiaSíndrome de Kaplowitz-Bodurtha
itIpopituitarismo - microftalmiaSindrome di Kaplowitz-Bodurtha
nlHypopituïtarisme - microftalmie-syndroomSyndroom van Kaplowitz-Bodurtha
ptSíndrome de hipopituitarismo-microftalmiaSíndrome Kaplowitz-Bodurtha
plNiedoczynność przysadki - małooczeZespół Kaplowitza i Bodurtha
csSyndrom zahrnující hypopituitarismus a mikroftalmiiKaplowitzův-Bodurthův syndrom · Kaplowitz-Bodurthův syndrom
ukСиндром гіпопітуїтаризму-мікрофтальміїСиндром Капловіца-Бодурта
zh垂体功能减退-小眼畸形综合征Kaplowitz-Bodurtha综合征
trHipopituitarizm-mikroftalmi sendromuKaplowitz-Bodurtha sendromu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC2931361Evalidated

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