raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2454

OBSOLETE: Familial intestinal malrotation-facial anomalies syndrome

inactive · referred to ORPHA:508410Familial intestinal malrotation

Synonyms: OBSOLETE: Stalker-Chitayat 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 Familial intestinal malrotation

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Familial intestinal malrotation-facial anomalies syndromeOBSOLETE: Stalker-Chitayat syndrome
frOBSOLETE : Syndrome familial de malrotation intestinale-dysmorphieOBSOLETE : Syndrome de Stalker-Chitayat
deOBSOLET: Familiäre syndromale intestinale Malrotation mit GesichtsanomalienOBSOLET: Stalker-Chitayat-Syndrom
esOBSOLETO: Síndrome familiar de malrotación intestinal-anomalías facialesOBSOLETO: Síndrome de Stalker-Chitayat
itOBSOLETO: Sindrome malrotazione intestinale familiare-anomalie faccialiOBSOLETO: Sindrome di Stalker-Chitayat
nlOBSOLEET: Familiaal intestinale malrotatie - faciale anomalieën-syndroomOBSOLEET: Syndroom van Stalker-Chitayat
ptOBSOLETO: Síndrome de malrotação intestinal-anomalias faciais familiarOBSOLETO: Síndrome Stalker-Chitayat
plNIEAKTUALNE: Rodzinna malrotacja jelit - wady twarzyNIEAKTUALNE: Zespół Stalkera i Chitayata
csNEAKTUÁLNÍ: Syndrom zahrnující familiární intestinální malrotaci a obličejové anomálieNEAKTUÁLNÍ: Stalkerův-Chitayatův syndrom · NEAKTUÁLNÍ: Stalker-Chitayatův syndrom
ukЗАСТАРІЛО: Сімейний синдром кишкової мальротації-лицевих аномалійЗАСТАРІЛО: Синдром Сталкера-Читаята
zh弃用:家族遗传性肠道转位异常-面部异常综合征Stalker-Chitayat综合征
trEski adı: ailesel bağırsak malrotasyonu-yüz anomalileri sendromuStalker-Chitayat 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