raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3228

OBSOLETE: Neurosensory deafness-pituitary dwarfism syndrome

inactive · referred to ORPHA:231720Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome

Synonyms: OBSOLETE: Neurosensory hearing loss-pituitary dwarfism syndrome · OBSOLETE: Winkelmann-Bethge-Pfeiffer syndrome

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Neurosensory deafness-pituitary dwarfism syndromeOBSOLETE: Neurosensory hearing loss-pituitary dwarfism syndrome · OBSOLETE: Winkelmann-Bethge-Pfeiffer syndrome
frOBSOLETE : Syndrome de surdité neurosensorielle-nanisme pituitaireOBSOLETE : Syndrome de Winkelmann-Bethge-Pfeiffer
deOBSOLET: Neurosensorische Schwerhörigkeit-hypophysärer Kleinwuchs-SyndromOBSOLET: Winkelman-Bethge-Pfeiffer-Syndrom
esOBSOLETO: Síndrome de sordera neurosensorial-talla baja significativa pituitariaOBSOLETO: Síndrome de Winkelmann-Bethge-Pfeiffer · OBSOLETO: Síndrome de hipoacusia neurosensorial-talla baja significativa pituitaria
itOBSOLETO: Sindrome sordità neurosensoriale-nanismo ipofisarioOBSOLETO: Sindrome perdita dell'udito neurosensoriale-nanismo ipofisario · OBSOLETO: Sindrome di Winkelman-Bethge-Pfeiffer
nlOBSOLEET: Neurosensorische doofheid - hypofysaire dwerggroei-syndroomOBSOLEET: Neurosensorisch gehoorverlies - hypofysaire dwerggroei-syndroom · OBSOLEET: Syndroom van Winkelmann-Bethge-Pfeiffer
ptOBSOLETO: Síndrome de surdez neuro-sensitiva-nanismo pituitárioOBSOLETO: Síndrome Winkelman-Bethge-Pfeiffer
plNIEAKTUALNE: Gluchota nerwowo-czuciowa - karlowatosc przysadkowaNIEAKTUALNE: Nerwowo-czuciowa utrata słuchu - karłowatość przysadkowa · NIEAKTUALNE: Zespół Winkelmanna, Bethge'a i Pfeiffera
csNEAKTUÁLNÍ: Syndrom neurosenzorické hluchoty a hypofyzárního trpaslictví= en
ukЗАСТАРІЛО: Синдром нейросенсорної глухоти-гіпофізарної карликовостіСиндром нейросенсорної приглухуватості-гіпофізарної карликовості · ЗАСТАРІЛО: Синдром Вінкельмана-Бетге-Пфайффера
zh弃用:神经感音性耳聋-垂体性侏儒症综合征感音神经性听力丧失-垂体性侏儒综合征
trEski adı: Nörosensoriyel sağırlık-hipofiz cücelik sendromuWinkelmann-Bethge-Pfeiffer sendromu · Nörosensoriyel işitme kaybı-hipofiz cücelik 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