Hyperphalangy (Q46463): Difference between revisions
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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
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dki-india-LB77
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