We publish our audit record because accuracy claims should be checkable. Every entry on this site runs through an automated fact-audit pipeline (accuracy audit → source-grounded repair → visual QA); this page is generated from that pipeline's own report, not written by hand.
Last full accuracy audit: 2026-09-08 · 31 entries checked · 12 flagged · 19 issues confirmed · 12 corrected · 7 still open
Aarskog–Scott syndrome — The DID YOU KNOW section claims 'Growth hormone trials have been effective to treat short stature in this disorder,' which is misleading and not a widely established fact; growth hormone therapy is not universally accepted as effective or standard treatment fo
Aase syndrome — The claim that 45% of cases are due to a change in one gene which makes ribosomal proteins is not established for Aase syndrome; this appears to be a confusion with Diamond-Blackfan anemia.
Adducted thumb syndrome — The entry conflates Christian's original 1971 syndrome (adducted thumbs with cleft palate) with the distinct CHST14-related disorder now classified as musculocontractural Ehlers-Danlos syndrome (mcEDS), which was described later by others.
Adducted thumb syndrome — The claim that cognitive development is typically normal is inconsistent because it mixes the normal cognition of CHST14-related mcEDS with the frequent intellectual disability of Christian's original syndrome.
Albright's hereditary osteodystrophy — The LORE section states that 'Martin-Albright syndrome' refers to Eric Martin, but it actually refers to John Martin and is a different condition (pseudohypoparathyroidism with hypogonadism and brachydactyly).
Alexander disease — Zilganersen (Zanvastro) was approved for medical use in the United States in September 2026
Allan–Herndon–Dudley syndrome — The claim that maternal ingestion of silymarin/silychristin during pregnancy can cause Allan–Herndon–Dudley syndrome is not established canon; AHDS is a genetic disorder caused by inherited mutations in SLC16A2, not an acquired condition from environmental exp
Batten disease — The entry states 'The CLN3 gene sits on the short arm of chromosome 16 at position 12.1', but the correct cytogenetic location is 16p12.1 (not '12.1' without the 'p' prefix).
Batten disease — The entry states 'About 73% of cases involve a specific 1.02-kb deletion', but the widely accepted figure is that the 1.02-kb deletion accounts for approximately 73% of mutant alleles in juvenile NCL, not 73% of cases (some cases are compound heterozygotes wit
Bruck syndrome — The entry incorrectly states the patient was male; the first patient described by Alfred Bruck in 1897 was female.
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