DNA-ligase IV deficiency (Q88881): Difference between revisions

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+https://id.who.int/icd/entity/969767034
@@ Property / Canonical URI: https://id.who.int/icd/entity/969767034 / rank @@
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+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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++2026-08-13T00:00:00Z
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@@ Property / Collection date: 13 August 2026 / rank @@
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Latest revision as of 15:16, 15 August 2026

LIG4 syndrome is a hereditary disorder associated with impaired DNA double strand break repair mechanisms and characterised by microcephaly, unusual facial features, growth and developmental delay, skin anomalies, and pancytopenia, which is associated with combined immunodeficiency (CID).

Language	Label	Description	Also known as
default for all languages	ID_969767034
English	DNA-ligase IV deficiency	LIG4 syndrome is a hereditary disorder associated with impaired DNA double strand break repair mechanisms and characterised by microcephaly, unusual facial features, growth and developmental delay, skin anomalies, and pancytopenia, which is associated with combined immunodeficiency (CID).