ORPHA:1250

OBSOLETE: Blaichman syndrome

inactive · referred to ORPHA:102285Multiple congenital anomalies/dysmorphic syndrome without intellectual disability

Synonyms: OBSOLETE: Tracheo-esophageal fistula-symphalangism 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 Multiple congenital anomalies/dysmorphic syndrome without intellectual disability

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Blaichman syndrome	OBSOLETE: Tracheo-esophageal fistula-symphalangism syndrome
fr	OBSOLETE : Syndrome de Blaichman	OBSOLETE : Fistule trachéo-oesophagienne-symphalangie
de	OBSOLET: Blaichman-Syndrom	OBSOLET: Tracheo-ösophageale Fistel mit Symphalangie
es	OBSOLETO: Síndrome de Blaichman	OBSOLETO: Síndrome de fístula traqueoesofágica-sinfalangismo
it	OBSOLETO: Sindrome di Blaichman	OBSOLETO: Sindrome fistola tracheo-esofagea-sinfalangismo
nl	OBSOLEET: Syndroom van Blaichman	OBSOLEET: Tracheo-oesofageale fistel - symfalangisme-syndroom
pt	OBSOLETO: Síndrome Blaichman
pl	NIEAKTUALNE: Zespól Blaichmana	NIEAKTUALNE: Szczelina tchawiczo-przełykowa - symfalangizm
cs	NEAKTUÁLNÍ: Blaichmanův syndrom	= en
uk	ЗАСТАРІЛО: Синдром Блейхмана	Синдром трахео-стравохідної нориці-симфалангізму
zh	弃用：Blaichman 综合征	气管食管瘘-指骨关节融合综合征
tr	Eski adı: Blaichman sendromu	Trakeo-özofageal fistül-simfalanjizm sendromu

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Not placed in any Orphanet classification in this release.

No children.

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/1250
This record as JSON: /data/d/1250.json