Familial isolated clinodactyly of fingers
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
Familial isolated clinodactyly of fingers is a rare, genetic, non-syndromic, congenital limb malformation disorder characterized by angulation of a digit in the radio-ulnar (coronal) plane, away from the axis of joint flexion-extension, in several members of a single family with no other associated manifestations. Deviation is usually bilateral and commonly involves the fifth finger. Affected digits present trapezoidal or delta-shaped phalanges on imaging.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Familial isolated clinodactyly of fingers | |
| fr | Clinodactylie des doigts familiale isolée | |
| de | Isolierte Klinodaktylie der Finger, familiäre Form | |
| es | Clinodactilia familiar aislada de los dedos de la mano | |
| it | Clinodattilia isolata familiare delle dita delle mani | |
| nl | Familiale geïsoleerde clinodactylie van vinger | |
| pt | Clinodactilia isolada familiar dos dedos da mão | |
| pl | Rodzinna izolowana klinodaktylia palców dłoni | |
| cs | Familiární izolovaná klinodaktylie prstů ruky | |
| uk | Сімейна ізольована клинодактилія пальців рук | |
| zh | 家族性孤立性指曲畸形 | |
| tr | Ailesel izole klinodaktili parmaklar |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q68.1 | NTBT | attributed | validated |
| ICD-11 | LB80.0 | NTBT | attributed | validated |
| MONDO | 0017461 | E | validated | |
| UMLS | C4706540 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:294947Congenital deformities of fingers
rare developmental anomalies during embryogenesis; rare genetic diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/295014
- This record as JSON: /data/d/295014.json