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Article

Identification of Associated Genes and Diseases in Patients With Congenital Upper-Limb Anomalies: A Novel Application of the OMT Classification.

The Journal of hand surgery - 1 Jul 2017

Baas Martijn, Stubbs Andrew P, van Zessen David B, Galjaard Robert-Jan H, van der Spek Peter J, Hovius Steven E R, van Nieuwenhoven Christianne A

Abstract excerpt

PURPOSE: Congenital upper-limb anomalies (CULA) can present as a part of a syndrome or association. There is a wide spectrum of CULA, each of which might be related to different diseases. The structure provided by the Oberg, Manske, and Tonkin (OMT) classification could aid in differential diagnosis formulation in patients with CULA. The aims of this study were to review the Human Phenotype Ontology (HPO) project...

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Identifiers

PMID: 28669419
DOI: 10.1016/j.jhsa.2017.03.043

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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