"Singleton Merten syndrome" meaning in English

See Singleton Merten syndrome in All languages combined, or Wiktionary

Noun

Head templates: {{en-noun|-}} Singleton Merten syndrome (uncountable)
  1. An autosomal-dominant genetic disorder with variable expression with an onset of symptoms during childhood. Tags: uncountable
    Sense id: en-Singleton_Merten_syndrome-en-noun-dtnHXusM Categories (other): English entries with incorrect language header, Pages with 1 entry, Pages with entries
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        "An autosomal-dominant genetic disorder with variable expression with an onset of symptoms during childhood."
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This page is a part of the kaikki.org machine-readable English dictionary. This dictionary is based on structured data extracted on 2026-09-06 from the enwiktionary dump dated 2026-09-02 using wiktextract (ccec6f1 and 4deed51). The data shown on this site has been post-processed and various details (e.g., extra categories) removed, some information disambiguated, and additional data merged from other sources. See the raw data download page for the unprocessed wiktextract data.

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