raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:295065

OBSOLETE: Femoral agenesis/hypoplasia, unilateral

inactive · referred to ORPHA:1987Isolated femoral agenesis/hypoplasia

Synonyms: OBSOLETE: Femoral intercalary meromelia, unilateral

Type
Clinical subtype
Group
Subtype of disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Isolated femoral agenesis/hypoplasia

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Femoral agenesis/hypoplasia, unilateralOBSOLETE: Femoral intercalary meromelia, unilateral
frOBSOLETE : Agénésie/hypoplasie unilatérale du fémurOBSOLETE : Agénésie/hypoplasie unilatérale du fémorale · OBSOLETE : Méromélie intercalaire unilatérale du fémorale · OBSOLETE : Méromélie intercalaire unilatérale du fémur
deOBSOLET: Femuragenesie/-hypoplasie, unilateralOBSOLET: Femorale interkalare Meromelie, unilateral
esOBSOLETO: Agenesia/hipoplasia femoral unilateralOBSOLETO: Meromelia intercalar femoral unilateral
itOBSOLETO: Agenesia/ipoplasia del femore, unilateraleOBSOLETO: Meromelia intercalare del femore, unilaterale
nlOBSOLEET: Femorale agenesie/hypoplasie, unilateraalOBSOLEET: Femorale intercalaire meromelie, unilateraal
ptOBSOLETO: Agenesia/hipoplasia femoral, unilateralOBSOLETO: Meromelia intercalar femoral, unilateral
plNIEAKTUALNE: Agenezja/hipoplazja kosci udowej, jednostronna= en
csNEAKTUÁLNÍ: Jednostranná ageneze/hypoplázie femuruNEAKTUÁLNÍ: Jednostranná interkalární meromelie femuru
ukЗАСТАРІЛО: Агенезія/гіпоплазія стегнової кістки, односторонняЗАСТАРІЛО: Стегнова інтеркалярна меромелія, однобічна
zh弃用:单侧股骨发育不全/发育不良单侧股骨骨干残肢畸形
trEski adı: Femoral agenezi / hipoplazi, unilateralFemoral interkalar meromeli, unilateral
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