Mucolipidosis type 4 (Q58520): Difference between revisions

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13 August 2026
Timestamp+2026-08-13T00:00:00Z
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Latest revision as of 06:05, 14 August 2026

Mucolipidosis type IV (ML IV) is a lysosomal storage disease characterised clinically by psychomotor retardation and visual abnormalities including corneal clouding, retinal degeneration, or strabismus.
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ID_597963317
    English
    Mucolipidosis type 4
    Mucolipidosis type IV (ML IV) is a lysosomal storage disease characterised clinically by psychomotor retardation and visual abnormalities including corneal clouding, retinal degeneration, or strabismus.

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      CID11:ID_597963317
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      dki-india-ID_597963317
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      Concluído
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      13 August 2026
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