raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:601018

Non-syndromic rectal atresia

Synonyms: Non-syndromic ARM with rectal atresia · Non-syndromic anorectal malformation with rectal atresia

Type
Morphological anomaly
Group
Disorder
Age of onset
Neonatal
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enNon-syndromic rectal atresiaNon-syndromic ARM with rectal atresia · Non-syndromic anorectal malformation with rectal atresia
frAtrésie rectale non syndromiqueARM non syndromique avec atrésie rectale · MAR non syndromique avec atrésie rectale · Malformation anorectale non syndromique avec atrésie rectale
deNicht-syndromale RektumatresieNicht-syndromale ARM mit Rektalatresie · Nicht-syndromale anorektale Fehlbildung mit Rektumatresie
esAtresia rectal no sindrómicaMAR no sindrómica con atresia rectal · Malformación anorrectal no sindrómica con atresia rectal
itAtresia del retto non sindromicaMalformazione anorettale non sindromica con atresia del retto · MAR non sindromica con atresia del retto
nlNiet-syndromale atresie van rectumNiet-syndromale atresie van endeldarm · Niet-syndromale ARM met atresie van rectum · Niet-syndromale anorectale malformatie met atresie van rectum
ptMalformação anorrectal não-sindromática com atrésia rectal
plNiesyndromiczna atrezja odbytnicy= en
csNesyndromická anorektální malformace s atrézií rekta= en
ukНесиндромальна аноректальна вада розвитку з атрезією прямої кишкиНесиндромальна ARM з атрезією прямої кишки
zhNon-syndromic anorectal malformation with rectal atresiaNon-syndromic ARM with rectal atresia
trNon-syndromic anorectal malformation with rectal atresiaNon-syndromic ARM with rectal atresia
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10Q42.0NTBTattributedvalidated
ICD-11LB17.0NTBTattributedvalidated
MONDO0035790Evalidated
UMLSC5680235Evalidated

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

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

2 records
TypeClassValueAreaQualificationValidationSource
Prevalence at birthUnknown—WorldwideClass onlyValidated16226976[PMID]_31194415[PMID]_ORPHANET
Point prevalenceUnknown—WorldwideClass onlyValidated16226976[PMID]_31194415[PMID]_ORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

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

7

Sources for this card