ORPHA:295201

Congenital vertical talus, unilateral

This disease is described under Congenital vertical talus

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Congenital vertical talus, unilateral
fr	Pied convexe congénital unilatéral	Pied en piolet congénital unilatéral
de	Talus verticalis, kongenital, unilateral
es	Astrágalo vertical congénito unilateral
it	Talo verticale congenito unilaterale
nl	Congenitale verticale talus, unilateraal
pt	Talo vertical congénito, unilateral
pl	Wrodzona stopa płasko-koślawa, jednostronna
cs	Unilaterální vrozený vertikální talus
uk	Вроджена вертикальна таранна кістка, одностороння
zh	先天性单侧垂直距骨
tr	Doğumsal vertikal talus, unilateral

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
OMIM	192950	NTBT		validated
ICD-10	Q66.8	NTBT	attributed	validated
ICD-11	LB98.4	NTBT	index	validated
MONDO	0017546	E		validated
UMLS	C5681089	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:178382Congenital vertical talus
rare developmental anomalies during embryogenesis; rare genetic diseases

No children.

1 direct

Gene	Association	Status	HGNC	Ensembl	OMIM	Locus	Name	Source of validation
HOXD10	Disease-causing germline mutation(s) in	Assessed	HGNC:5133	ENSG00000128710	142984	2q31.1	homeobox D10

0 records

No prevalence record in this release.

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