raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1654

OBSOLETE: Natal teeth-intestinal pseudoobstruction-patent ductus syndrome

inactive · referred to ORPHA:99811Neuronal intestinal pseudoobstruction

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 Neuronal intestinal pseudoobstruction

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Natal teeth-intestinal pseudoobstruction-patent ductus syndrome
frOBSOLETE : Syndrome de dents néonatales-pseudo-obstruction intestinale-persistance du canal artériel
deOBSOLET: Konnatale Zähne-intestinale Pseudoobstruktion-persistierender Ductus arteriosus-Syndrom
esOBSOLETO: Síndrome de dientes natales-pseudoobstrucción intestinal-ductus persistente
itOBSOLETO: Denti neonatali - pseudo-ostruzione intestinale - dotto arterioso pervio
nlOBSOLEET: Geboortetanden - intestinale pseudo-obstructie - persisterende ductus-syndroom
ptOBSOLETO: Síndrome de dentes neonatais-pseudo-oclusão intestinal-canal patente
plNIEAKTUALNE: Zeby noworodkowe - pseudozaparcie jelit - przetrwaly przewód tetniczy
csNEAKTUÁLNÍ: Syndrom zahrnující natální zuby, střevní pseudoobstrukci a otevřenou Botallovu dučej
ukЗАСТАРІЛО: Синдром молочних зубів-кишкової псевдообструкції-протокової непрохідності
zh弃用:胎生牙-假性肠梗阻-导管未闭综合征
trEski adı: Natal dişler-intestinal psödoobstrüksiyon-patent duktus 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