Hyperphalangy (Q46463): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Linked ICD 10 | |||
| Property / Linked ICD 10: Q65-Q79 / rank | |||
Normal rank | |||
Latest revision as of 15:03, 13 August 2026
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LB77 |
||
| English | Hyperphalangy |
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. |
Statements
CID11:LB77
0 references
dki-india-LB77
0 references
Concluído
0 references
13 August 2026
0 references
