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      • abnormal craniofacial development

    • abnormal mandibular prominence morphology   MP:0010939   (0)
    Definition: any structural anomaly of the paired ventral prominences formed by bifurcation of the first pharyngeal arches in the embryo; the two prominences unite ventrally and fuse to form the mandible and lower lip [ISBN:0-683-40008-8];   [MGI annotations / genotypes]
      (No descendants that are mapped to MPD data)



    VT:0010939 (erythrocyte molecular composition trait) is numbered similarly to MP:0010939 but is over in the VT ontology (semantics may or may not be similar).

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