DNA-ligase IV deficiency (Q88881): Difference between revisions
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dki-india-ID_969767034 | |||||||||||||||
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13 August 2026
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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 |
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| 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). |
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CID11:ID_969767034
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dki-india-ID_969767034
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Concluído
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13 August 2026
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