# GeDiPNet Cluster 157 -- Pairs Within Cluster -- generated 2026-10-07 11:27:28
# Similarity: Jaccard index on shared curated genes (disease_gdp). Significance: upper-tail hypergeometric test, Benjamini-Hochberg FDR-corrected across all tested pairs. See scripts/build_related.php on gedipnet.bicnirrh.res.in. Data as of: 2026-10-07 16:50:39.
Disease A	Disease B	Similarity Score	Shared Genes	P-value	FDR Q-value
Auditory neuropathy	Pendred syndrome	0.08333	3	2.572e-7	1.752e-6
progressive microcephaly-seizures-cortical blindness-developmental delay syndrome	Sensorineural hearing loss thrombocytopenia syndrome	0.50000	1	6.494e-5	2.369e-4
Neonatal convulsions	Sensorineural hearing loss thrombocytopenia syndrome	0.25000	1	1.948e-4	5.331e-4
Neonatal convulsions	progressive microcephaly-seizures-cortical blindness-developmental delay syndrome	0.25000	1	1.948e-4	5.331e-4
Arthrogryposis with ectodermal dysplasia	Pendred syndrome	0.12500	1	4.546e-4	9.609e-4
hearing loss, autosomal recessive 116	Pendred syndrome	0.12500	1	4.546e-4	9.609e-4
Pendred syndrome	Sensorineural hearing loss thrombocytopenia syndrome	0.12500	1	4.546e-4	9.609e-4
Pendred syndrome	progressive microcephaly-seizures-cortical blindness-developmental delay syndrome	0.12500	1	4.546e-4	9.609e-4
Arthrogryposis with ectodermal dysplasia	Auditory neuropathy	0.03125	1	2.013e-3	2.892e-3
Auditory neuropathy	Deafness dystonia syndrome	0.03125	1	2.013e-3	2.892e-3
Auditory neuropathy	progressive microcephaly-seizures-cortical blindness-developmental delay syndrome	0.03125	1	2.013e-3	2.892e-3
Auditory neuropathy	Sensorineural hearing loss thrombocytopenia syndrome	0.03125	1	2.013e-3	2.892e-3