Kocher-Debre-Semelaigne syndrome (Q106070): Difference between revisions

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Property / Collection date
 
16 August 2026
Timestamp+2026-08-16T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 16 August 2026 / rank
 
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Latest revision as of 12:51, 17 August 2026

This is a (myopathy) of hypothyroidism in infancy or childhood characterised by lower extremity or generalised muscular hypertrophy, myxoedema, short stature and cretinism.
Language Label Description Also known as
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ID_109007822
    English
    Kocher-Debre-Semelaigne syndrome
    This is a (myopathy) of hypothyroidism in infancy or childhood characterised by lower extremity or generalised muscular hypertrophy, myxoedema, short stature and cretinism.

      Statements

      CID11:ID_109007822
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      dki-india-ID_109007822
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      Concluído
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      16 August 2026
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