17q12 Knowledge Basedeletion syndrome · static snapshot
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Phenotype expansion Signs & symptoms 1 supporting source confidence 97% novelty 90%

New observation reported: Chen S., Sun Y., Fan Y., et al., "HOXD10: A Novel Gene Implicated in Human Müllerian Duct Anomalies," European…

A source describes a new or expanded observation: “Chen S., Sun Y., Fan Y., et al., "HOXD10: A Novel Gene Implicated in Human Müllerian Duct Anomalies," European Journal of Obstetrics, Gynecology, and Reproductive Biology 308 (2025): 6-14.”

How this was derived

Flagged by novelty language (“for the first time”, “expands the phenotype”, …) in pmc.

Generated 2026-11-13, last changed yesterday. Dedup key expansion:f2c919. 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)

Chen S., Sun Y., Fan Y., et al., "HOXD10: A Novel Gene Implicated in Human Müllerian Duct Anomalies," European Journal of Obstetrics, Gynecology, and Reproductive Biology 308 (2025): 6-14.

Supporting documents (1)

ArticleSourcePublishedSeenRelevance
The Genetic Landscape of Müllerian Duct Anomalies: A Comprehensive Review pmc 2025-01-01 yesterday 1.00