Hyperphalangy (Q46463): Difference between revisions

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@@ Property / CURIE: CID11:LB77 / rank @@
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Calendar Gregorian
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@@ Property / Collection date: 13 August 2026 / rank @@
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+Q65-Q79
@@ Property / Linked ICD 10: Q65-Q79 / rank @@
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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.