# GeDiPNet Cluster 70 -- Pairs Within Cluster -- generated 2026-10-07 02:05:04
# 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 03:00:13.
Disease A	Disease B	Similarity Score	Shared Genes	P-value	FDR Q-value
Bronchiectasis	Pseudohypoparathyroidism	0.14815	4	7.224e-10	7.016e-9
Liddle syndrome	Pseudohypoparathyroidism	0.20000	3	1.880e-9	1.746e-8
Bronchiectasis	Liddle syndrome	0.15789	3	4.468e-9	4.004e-8
familial juvenile hyperuricemic nephropathy type 2	renal tubular dysgenesis of genetic origin	0.50000	1	6.494e-5	2.342e-4
renal tubular dysgenesis of genetic origin	Tonne-kalscheuer syndrome	0.33333	1	1.299e-4	3.898e-4
familial juvenile hyperuricemic nephropathy type 2	Juvenile hyperuricemic nephropathy	0.33333	1	1.299e-4	3.898e-4
familial juvenile hyperuricemic nephropathy type 2	Tonne-kalscheuer syndrome	0.33333	1	1.299e-4	3.898e-4
Juvenile hyperuricemic nephropathy	renal tubular dysgenesis of genetic origin	0.33333	1	1.299e-4	3.898e-4
familial juvenile hyperuricemic nephropathy type 2	Malignant hypertension	0.25000	1	1.948e-4	5.278e-4
Malignant hypertension	renal tubular dysgenesis of genetic origin	0.25000	1	1.948e-4	5.278e-4
Juvenile hyperuricemic nephropathy	Tonne-kalscheuer syndrome	0.25000	1	2.598e-4	6.403e-4
Liddle syndrome	pseudohypoaldosteronism, type IB1, autosomal recessive	0.20000	1	2.598e-4	6.403e-4
Liddle syndrome	renal tubular dysgenesis of genetic origin	0.20000	1	2.598e-4	6.403e-4
familial juvenile hyperuricemic nephropathy type 2	Liddle syndrome	0.20000	1	2.598e-4	6.403e-4
Malignant hypertension	Tonne-kalscheuer syndrome	0.20000	1	3.896e-4	8.521e-4
Juvenile hyperuricemic nephropathy	Liddle syndrome	0.16667	1	5.195e-4	1.041e-3
Liddle syndrome	Tonne-kalscheuer syndrome	0.16667	1	5.195e-4	1.041e-3
pseudohypoaldosteronism type 2D	Pseudohypoparathyroidism	0.07143	1	8.443e-4	1.478e-3
pseudohypoaldosteronism type 2E	Pseudohypoparathyroidism	0.07143	1	8.443e-4	1.478e-3
pseudohypoaldosteronism, type IB1, autosomal recessive	Pseudohypoparathyroidism	0.07143	1	8.443e-4	1.478e-3
Portal hypertension	renal tubular dysgenesis of genetic origin	0.06250	1	9.742e-4	1.644e-3
familial juvenile hyperuricemic nephropathy type 2	Portal hypertension	0.06250	1	9.742e-4	1.644e-3
Bronchiectasis	pseudohypoaldosteronism, type IB1, autosomal recessive	0.05556	1	1.104e-3	1.805e-3
Bronchiectasis	congenital disorder of glycosylation, type 2v	0.05556	1	1.104e-3	1.805e-3
