raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:480773

OBSOLETE: Fibular aplasia-tibial campomelia-oligosyndactyly syndrome

inactive · referred to ORPHA:2492FATCO syndrome

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 FATCO syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Fibular aplasia-tibial campomelia-oligosyndactyly syndrome
frOBSOLETE : Syndrome d'aplasie fibulaire-campomélie tibiale-oligosyndactylieOBSOLETE : Syndrome FATCO
deOBSOLET: Fibula-Aplasie-Tibia-Kampomelie-Oligosyndaktylie-SyndromOBSOLET: FATCO-Syndrom
esOBSOLETO: Síndrome de aplasia fibular-campomelia tibial-oligosindactiliaOBSOLETO: Síndrome FATCO
itOBSOLETO: Fibular aplasia-tibial campomelia-oligosyndactyly syndrome
nlOBSOLEET: Fibulaire aplasie - tibiale campomelie - oligosyndactylie-syndroomOBSOLEET: FATCO-syndroom
ptOBSOLETO: Síndrome de aplasia da fíbula-campomelia da tíbia-oligosindactiliaOBSOLETO: Síndrome FATCO
plNIEAKTUALNE: Zespól aplazji kosci strzalkowej, wygiecia kosci piszczelowej i oligosyndaktyliiNIEAKTUALNE: Zespół FATCO
csNEAKTUÁLNÍ: Syndrom zahrnující fibulární aplázii, tibiální kampomelii a oligosyndaktylii
ukСиндром фіброзної аплазії-кампомелії великогомілкової кістки-олігосиндактилії
zh已废除:腓骨发育不全-胫骨弯曲带-单并指综合征
trEski adı: Fibular aplazi-tibial campomelia-oligosindaktili 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