raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2864

OBSOLETE: Short stature-prognathism-short femoral necks syndrome

inactive · referred to ORPHA:364526Primary bone dysplasia

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 Primary bone dysplasia

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Short stature-prognathism-short femoral necks syndrome
frOBSOLETE : Syndrome de petite taille-prognathisme-fémur court
deOBSOLET: Kleinwuchs - Prognathie - kurzer Oberschenkelhals
esOBSOLETO: Síndrome de talla baja-prognatismo-fémur corto
itOBSOLETO: Bassa statura - prognatismo - femore corto
nlOBSOLEET: Kleine gestalte - prognathie - korte femurhals-syndroom
ptOBSOLETO: Síndrome de baixa estatura-prognatismo-colo do fémur curto
plNIEAKTUALNE: Niski wzrost - prognatyzm - krótkie szyjki kosci udowych
csNEAKTUÁLNÍ: Syndrom zahrnující malý vzrůst, prognatismus a krátký krček stehenní kosti
ukЗАСТАРІЛО: Синдром низькорослості - прогнатизму - короткої шийки стегнових кісток
zh弃用:身材矮小-下颌前突-短股骨颈综合征
trEski adı: Kısa boy-öne çıkık çene-kısa femoral boyun 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