ORPHA:601008

Non-syndromic anal stenosis

Synonyms: Non-syndromic ARM with anal stenosis · Non-syndromic anorectal malformation with anal stenosis

Orphadata ships no English definition for this code.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Non-syndromic anal stenosis	Non-syndromic ARM with anal stenosis · Non-syndromic anorectal malformation with anal stenosis
fr	Sténose anale non syndromique	ARM non syndromique avec sténose anale · MAR non syndromique avec sténose anale · Malformation anorectale non syndromique avec sténose anale
de	Nicht-syndromale Analstenose	Nicht-syndromale ARM mit Analstenose · Nicht-syndromale anorektale Fehlbildung mit Analstenose
es	Estenosis anal no sindrómica	MAR no sindrómica con estenosis anal · Malformación anorrectal no sindrómica con estenosis anal
it	Stenosi anale non sindromica	MAR non sindromica con stenosi anale · Malformazione anorettale non sindromica con stenosi anale
nl	Niet-syndromale stenose van anus	Niet-syndromale ARM met stenose van anus · Niet-syndromale anorectale malformatie met stenose van anus
pt	Malformação anorrectal não-sindromática com estenose anal
pl	Niesyndromiczne zwężenie odbytu	= en
cs	Nesyndromická anorektální malformace s anální stenózou	= en
uk	Несиндромальна аноректальна вада розвитку з анальним стенозом	Несиндромальна ARM з анальним стенозом
zh	Non-syndromic anorectal malformation with anal stenosis	Non-syndromic ARM with anal stenosis
tr	Non-syndromic anorectal malformation with anal stenosis	Non-syndromic ARM with anal stenosis

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	Q42.3	NTBT	attributed	validated
ICD-11	LB17.0	NTBT	attributed	validated
MONDO	0035788	E		validated
UMLS	C5680233	E		validated

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

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

ORPHA:557Non-syndromic anorectal malformation
rare developmental anomalies during embryogenesis; rare genetic diseases; rare abdominal surgical diseases; rare transplant-related disorders

No children.

0 direct

Orphanet records no gene directly on this code.

2 records

Type	Class	Value	Area	Qualification	Validation	Source
Prevalence at birth	Unknown	—	Worldwide	Class only	Validated	16226976[PMID]_31194415[PMID]_ORPHANET
Point prevalence	Unknown	—	Worldwide	Class only	Validated	16226976[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.

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