17q12, explained for kidsdeletion syndrome · static snapshot
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A new article Genes and families 1 supporting source confidence 97% novelty 75%

Novel compound heterozygous mutation in DNAH9 causes complex congenital heart disease DNAH9 causes complex congenital heart disease

Congenital heart disease (CHD) is the most common birth defect, affecting 2-8% of newborns, with a marked impact on neonatal health.

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How this was derived

Indexed from **pmc** on 2026-11-13 (relevance 1.00, tier peer_reviewed).

Generated 2026-11-13, last changed yesterday. Dedup key newdoc:368. The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.

Evidence (1 quote)

Novel compound heterozygous mutation in DNAH9 causes complex congenital heart disease DNAH9 causes complex congenital heart disease peer_reviewed · published 2025-01-01 · live page
Concurrent of compound heterozygous variant of a novel in-frame deletion and the common hypomorphic haplotype in TBX6 and inherited 17q12 microdeletion in a fetus.

Supporting documents (1)

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Novel compound heterozygous mutation in DNAH9 causes complex congen... pmc 2025-01-01 yesterday 1.00