ORPHA:2355

Kumar-Levick syndrome

Synonyms: Nail dysplasia-camptodactyly-brachydactyly type B syndrome

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Cooks syndrome

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Kumar-Levick syndrome	Nail dysplasia-camptodactyly-brachydactyly type B syndrome
fr	Syndrome de Kumar-Levick	Syndrome de dysplasie des ongles-camptodactylie-brachydactylie type B
de	Kumar-Levick-Syndrom	Anonychie - Onychodystrophie - Brachydaktylie Typ B - Ektrodaktylie
es	Síndrome de Kumar Levick	Anoniquia-onicodistrofia-braquidactilia tipo B-ectrodactilia
it	Sindrome di Kumar-Levick	Displasia ungueale - camptodattilia - brachidattilia tipo B
nl	Syndroom van Kumar-Levick	Nageldysplasie - camptodactylie - brachydactylie type B-syndroom
pt	Síndrome Kumar-Levick	Síndrome de anoníquia-onicodistrofia-braquidactilia tipo B
pl	Zespół Kumara i Levicka	Dysplazja paznokci - kamptodaktylia - brachydaktylia typu B
cs	Kumarův-Levickův syndrom	Syndrom zahrnující dysplázii nehtů, kamptodaktylii a brachydaktylii typu B · Kumar-Levickův syndrom
uk	Синдром Кумара-Левіка	Синдром дисплазії нігтів-камптодактилія-брахідактилія типу В
zh	Kumar-Levick综合征	指甲发育不良-屈曲指-B型短指综合征
tr	Kumar-Levick sendromu	Tırnak displazisi-kamptodaktili-brakidaktili tip B sendromu

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
OMIM	106990	E		validated

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

Not placed in any Orphanet classification in this release.

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

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