# GeDiPNet Cluster 188 -- Pairs Within Cluster -- generated 2026-10-07 22:55:47
# 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: 2026-10-08 03:00:12.
Disease A	Disease B	Similarity Score	Shared Genes	P-value	FDR Q-value
ACTB-associated syndromic thrombocytopenia	Congenital smooth muscle hamartoma	0.50000	1	6.494e-5	2.317e-4
ACTB-associated syndromic thrombocytopenia	Developmental malformations-deafness-dystonia syndrome	0.50000	1	6.494e-5	2.317e-4
ACTB-associated syndromic thrombocytopenia	Dystonia-deafness syndrome	0.50000	1	6.494e-5	2.317e-4
Developmental malformations-deafness-dystonia syndrome	Dystonia-deafness syndrome	0.50000	1	6.494e-5	2.317e-4
Congenital smooth muscle hamartoma	Dystonia-deafness syndrome	0.50000	1	6.494e-5	2.317e-4
Congenital smooth muscle hamartoma	Developmental malformations-deafness-dystonia syndrome	0.50000	1	6.494e-5	2.317e-4
Becker nevus syndrome	Dystonia-deafness syndrome	0.50000	1	6.494e-5	2.317e-4
Becker nevus syndrome	Developmental malformations-deafness-dystonia syndrome	0.50000	1	6.494e-5	2.317e-4
Becker nevus syndrome	Congenital smooth muscle hamartoma	0.50000	1	6.494e-5	2.317e-4
ACTB-associated syndromic thrombocytopenia	Becker nevus syndrome	0.50000	1	6.494e-5	2.317e-4
Baraitser-winter cerebrofrontofacial syndrome	Developmental malformations-deafness-dystonia syndrome	0.33333	1	1.299e-4	3.908e-4
Baraitser-winter cerebrofrontofacial syndrome	Dystonia-deafness syndrome	0.33333	1	1.299e-4	3.908e-4
Baraitser-winter cerebrofrontofacial syndrome	Congenital smooth muscle hamartoma	0.33333	1	1.299e-4	3.908e-4
Baraitser-winter cerebrofrontofacial syndrome	Becker nevus syndrome	0.33333	1	1.299e-4	3.908e-4
ACTB-associated syndromic thrombocytopenia	Baraitser-winter cerebrofrontofacial syndrome	0.33333	1	1.299e-4	3.908e-4
ACTB-associated syndromic thrombocytopenia	Aminoacylase deficiency	0.20000	1	2.598e-4	6.484e-4
Aminoacylase deficiency	Dystonia-deafness syndrome	0.20000	1	2.598e-4	6.484e-4
Aminoacylase deficiency	Developmental malformations-deafness-dystonia syndrome	0.20000	1	2.598e-4	6.484e-4
Aminoacylase deficiency	Congenital smooth muscle hamartoma	0.20000	1	2.598e-4	6.484e-4
Aminoacylase deficiency	Becker nevus syndrome	0.20000	1	2.598e-4	6.484e-4
Becker nevus syndrome	Dysphoric mood	0.20000	1	2.598e-4	6.484e-4
Congenital smooth muscle hamartoma	Dysphoric mood	0.20000	1	2.598e-4	6.484e-4
Developmental malformations-deafness-dystonia syndrome	Dysphoric mood	0.20000	1	2.598e-4	6.484e-4
Dysphoric mood	Dystonia-deafness syndrome	0.20000	1	2.598e-4	6.484e-4
ACTB-associated syndromic thrombocytopenia	Dysphoric mood	0.20000	1	2.598e-4	6.484e-4