Isolated hyperphalangy
Synonyms: Isolated congenital supernumerary phalanges · Supernumerary phalanx
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
Hyperphalangy is a congenital, non-syndromic limb malformation characterized by the presence of an accessory phalanx between metacarpal/metatarsal and proximal phalanx, or between any two other phalanges of a digit, excluding the thumb. Hypherphalangy is almost always bilateral and patients present no more than five digits and no other skeletal anomalies.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated hyperphalangy | Isolated congenital supernumerary phalanges · Supernumerary phalanx |
| fr | Hyperphalangie isolée | Phalange surnuméraire congénitale isolée |
| de | Hyperphalangie, isolierte | Isolierte angeborene überzählige Phalangen · Isoliertes überzähliges Finger-/Zehenglied |
| es | Hiperfalangia aislada | Falange supernumeraria · Falanges supernumerarias congénitas aisladas |
| it | Iperfalangia isolata | Falange soprannumeraria · Falangi congenite isolate soprannumerarie |
| nl | Geïsoleerde hyperfalangie | Geïsoleerde congenitale overtallige falangen · Geïsoleerde congenitale surnumeraire falangen · Surnumeraire falanx |
| pt | Hiperfalangismo isolado | Falange supernumerária isolada congénita · Falanges supernumerárias |
| pl | Paliczki dodatkowe | Paliczek dodatkowy · Paliczki dodatkowe · Izolowana hiperfalangia |
| cs | Hyperfalangie | Nadpočetné články prstů · Nadpočetný článek prstu |
| uk | Ізольована гіперфалангія | Ізольовані вроджені додаткові фаланги · Додаткова фаланга |
| zh | 多指/趾 | 多指/趾骨 |
| tr | Hiperfalanji | Süpernümerari falanks · Süpernümerari falankslar |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q74.8 | NTBT | attributed | validated |
| ICD-11 | LB77 | E | specific | validated |
| MONDO | 0017455 | E | validated | |
| UMLS | C4706507 | 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:93458Non-syndromic polydactyly, syndactyly and/or hyperphalangy
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases
No children.
Codes that Orphanet moved or referred to this one:
- ORPHA:295140OBSOLETE: Hyperphalangy, unilateral referred to · inactive
- ORPHA:295142OBSOLETE: Hyperphalangy, bilateral referred to · inactive
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/295002
- This record as JSON: /data/d/295002.json