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      • abnormal retinal photoreceptor morphology

    • abnormal retinal cone cell morphology   MP:0001006   (3)
    Definition: any structural anomaly of one of the photoreceptor cell types in the retina, in which the photopigment is in invaginations of the cell membrane of the outer segment; cones are less sensitive to light than rods, but they provide vision with higher spatial and temporal acuity, and the combination of signals from cones with different pigments allows color vision [MESH:A08.663.650.650.670.100]; xref: CL:0000573;   [MGI annotations / genotypes]
      (No descendants that are mapped to MPD data)



    VT:0001006 (retinal cone cell morphology trait) is numbered similarly to MP:0001006 but is over in the VT ontology (semantics may or may not be similar).

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