raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:995

X-linked fetal akinesia syndrome

inactive · moved to ORPHA:994Fetal akinesia deformation sequence

Synonyms: Holmes-Benacerraf syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Fetal akinesia deformation sequence

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enX-linked fetal akinesia syndromeHolmes-Benacerraf syndrome
frSyndrome d'akinésie foetale lié à l'XSyndrome de Holmes-Benacerraf
deFetales Akinesie-Syndrom, X-chromosomalesHolmes-Benacerraf-Syndrom
esSíndrome de aquinesia fetal ligada al cromosoma XSíndrome de Holmes-Benacerraf
itSindrome da acinesia fetale, legata all'XSindrome di Holmes-Benacerraf
nlX-gebonden foetale akinesiesyndroomHolmes-Benacerrafsyndroom
ptSíndrome acinesia fetal ligada ao X
plZespół akinezji płodu sprzężony z chromosomem XZespół Holmesa i Benacerrafa
csX-vázaná fetální akinezeHolmesův-Benacerrafové syndrom · Holmes-Benacerrafové syndrom
ukХ-зчеплений синдром акінезії плодаСиндром Холмса-Бенасеррафа
zhX连锁致死性运动失能综合征Holmes-Benacerraf 综合征
trX'e bağlı fetal akinezi sendromuHolmes-Benacerraf sendromu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC1848171Evalidated

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

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