raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:667589

Isolated congenital femoral bifurcation

Synonyms: Isolated congenital distal femoral duplication

Type
Morphological anomaly
Group
Disorder
Inheritance
Unknown
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

10 of 12 languages
LangNameSynonyms
enIsolated congenital femoral bifurcationIsolated congenital distal femoral duplication
frDuplication fémorale congénitale isolée
deFemoralbifurkation, isolierte kongenitaleIsolierte angeborene distale Oberschenkelduplikation
esBifurcación femoral congénita aisladaDuplicación femoral distal congénita aislada
itBiforcazione congenita isolata del femoreDuplicazione congenita isolata della porzione distale del femore
nlGeïsoleerde congenitale bifurcatie van femurGeïsoleerde congenitale bifurcatie van distale femur
ptBifurcação femoral isolada congénitaDuplicação femoral distal isolada congénita
plIsolated congenital femoral bifurcation= en
csIzolovaná vrozená bifurkace femuru= en
ukІзольоване вроджене роздвоєння стегнової кісткиІзольоване вроджене дистальне подвоєння стегнової кістки
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10Q74.2NTBTattributedvalidated
MONDO971109Evalidated
UMLSC5925060Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

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