LB77 Hyperphalangy
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2025-01
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.
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
synonyms
- Hyperphalangy
- Hyperphalangy, unilateral
- Hyperphalangy, bilateral
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