ORPHA:601033

Non-syndromic H-type fistula

Synonyms: Non-syndromic ARM with H-type fistula · Non-syndromic anorectal malformation with H-type fistula

Orphadata ships no English definition for this code.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Non-syndromic H-type fistula	Non-syndromic ARM with H-type fistula · Non-syndromic anorectal malformation with H-type fistula
fr	Fistule type H non syndromique	ARM non syndromique avec fistule type H · MAR non syndromique avec fistule type H · Malformation anorectale non syndromique avec fistule type H
de	Nicht-syndromale Fistel vom H-Fistel Typ	Nicht-syndromale ARM mit H-Fistel · Nicht-syndromale anorektale Fehlbildung mit H-Fistel
es	Fístula no sindrómica en H	MAR no sindrómica con fístula en H · Malformación anorrectal no sindrómica con fístula en H
it	Fistola tipo H non sindromica	Malformazione anorettale non sindromica con fistola di tipo H · MAR non sindromica con fistola di tipo H
nl	Niet-syndromale H-type fistel	Niet-syndromale ARM met H-type fistel · Niet-syndromale anorectale malformatie met H-type fistel
pt	Malformação anorrectal não-sindromática com fístula tipo H
pl	Niesyndromiczna przetoka typu H	= en
cs	Nesyndromická anorektální malformace s píštělí typu H	= en
uk	Несиндромальна аноректальна вада розвитку з норицею Н-типу	Несиндромальна ARM з норицею Н-типу
zh	Non-syndromic anorectal malformation with H-type fistula	Non-syndromic ARM with H-type fistula
tr	Non-syndromic anorectal malformation with H-type fistula	Non-syndromic ARM with H-type fistula

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	Q42.0	NTBT	attributed	validated
ICD-10	Q42.2	NTBT	attributed	validated
ICD-11	LB17.0	NTBT	attributed	validated
MONDO	0035793	E		validated
UMLS	C5680232	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.