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1p36 deletion syndrome

1p36 deletion syndrome noun: a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features.

Noun

1p36 deletion syndrome (uncountable)

  1. A congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features.

Questions about 1p36 deletion syndrome

What does 1p36 deletion syndrome mean?
1p36 deletion syndrome means a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features.
What part of speech is 1p36 deletion syndrome?
1p36 deletion syndrome is a noun.

Words near 1p36 deletion syndrome in the dictionary

  1. 1MR
  2. 1NCP
  3. 1NF
  4. 1OT
  5. 1OTs
  6. 1p36 deletion syndrome
  7. 1PL
  8. 1PP
  9. 1PPs
  10. 1s
  11. 1st

Source and license

Adapted from Wiktionary: 1p36 deletion syndrome (page history and authors). Text available under the Creative Commons Attribution-ShareAlike 4.0 license. Word.ws reformatted the entry and added links. Wiktionary data of 2026-09-02.

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Cite this entry: “1p36 deletion syndrome.” Word.ws, https://word.ws/1p36_deletion_syndrome. Based on Wiktionary, CC BY-SA 4.0.