Log in to save this analysis

Save This Analysis

What do these columns mean?
Shared genes
Curated genes linked to both diseases (disease_gdp). The line below it shows how many of those are "corroborated" -- backed by 2+ independent database sources combined across both diseases, not resting on a single source's say-so.
Similarity score
Jaccard-based: shared genes ÷ the union of both diseases' entire gene sets, with a small boost from users who bookmarked both diseases. Treats both diseases symmetrically.
Overlap coefficient
Shared genes ÷ the smaller disease's own total gene count. Complements the similarity score above for asymmetric pairs -- e.g. a rare disease almost entirely "contained" in a common disease's much larger gene set scores low on Jaccard but high here.
P-value / FDR q-value
Is this gene overlap more than chance? An upper-tail hypergeometric test, Benjamini-Hochberg corrected across every tested pair (the q-value is the one that accounts for testing thousands of pairs at once -- prefer it over the raw p-value).
Shared cluster
Links to a multi-disease cluster (see Disease Clusters) if both diseases of this pair were independently grouped together by that separate analysis.
ⓘ Shows only pairs whose gene overlap is too large to be down to chance (FDR q-value below 0.05). These are the rows marked ✓ sig. in the table. ⓘ Shows only pairs where both diseases also belong to the same group on the Disease Clusters page. Two separate analyses agree they're related, so the link is stronger. These are the rows with a link in the Shared cluster column.
0 selected Clear
Disease A ⇵Disease B ⇵Shared genes ⇵Similarity score ⇵Overlap coefficient ⇵P-value ⇵FDR q-value ▼ Shared cluster
Arginine vasopressin resistance Neurogenic diabetes insipidus
2 genes
Show details
2 of 2 corroborated by 2+ sources
AQP2(6), AVPR2(5)
0.400 1.000 5.06e-8 3.71e-7 ✓ sig. —
Arginine vasopressin resistance Nephrogenic diabetes insipidus
2 genes
Show details
2 of 2 corroborated by 2+ sources
AQP2(3), AVPR2(3)
0.400 1.000 5.06e-8 3.71e-7 ✓ sig. —
Iridogoniodysgenesis Rieger syndrome
2 genes
Show details
2 of 2 corroborated by 2+ sources
FOXC1(2), PITX2(3)
0.400 1.000 5.06e-8 3.71e-7 ✓ sig. Cluster 253 →
Dysphasia Postictal aphasia
2 genes
Show details
PLAT(1), L1CAM(1)
0.400 1.000 5.06e-8 3.71e-7 ✓ sig. Cluster 258 →
Dysphasia Syntactic aphasia
2 genes
Show details
PLAT(1), L1CAM(1)
0.400 1.000 5.06e-8 3.71e-7 ✓ sig. Cluster 258 →
Mainzer-saldino disease Saldino-mainzer syndrome
2 genes
Show details
2 of 2 corroborated by 2+ sources
IFT140(3), IFT172(2)
0.400 1.000 5.06e-8 3.71e-7 ✓ sig. Cluster 374 →
Mandibuloacral dysplasia Restrictive dermopathy
2 genes
Show details
2 of 2 corroborated by 2+ sources
LMNA(6), ZMPSTE24(7)
0.400 1.000 5.06e-8 3.71e-7 ✓ sig. Cluster 65 →
Multifocal osteomyelitis Recurrent multifocal osteomyelitis
2 genes
Show details
2 of 2 corroborated by 2+ sources
IL1R1(4), IL1RN(3)
0.400 1.000 5.06e-8 3.71e-7 ✓ sig. Cluster 216 →
Hyper-immunoglobulin d syndrome Mevalonate kinase deficiency
2 genes
Show details
1 of 2 corroborated by 2+ sources
MVK(4), HMGCR(1)
0.400 1.000 5.06e-8 3.71e-7 ✓ sig. Cluster 316 →
Hyper-immunoglobulin m syndrome Hyper-immunoglobulin syndrome
2 genes
Show details
AICDA(1), CD40(1)
0.400 1.000 5.06e-8 3.71e-7 ✓ sig. Cluster 131 →
Glanzmann thrombasthenia Thrombasthenia
2 genes
Show details
2 of 2 corroborated by 2+ sources
ITGB3(8), ITGA2B(8)
0.400 1.000 5.06e-8 3.71e-7 ✓ sig. Cluster 33 →
Gorlin syndrome nevoid basal cell carcinoma syndrome
2 genes
Show details
2 of 2 corroborated by 2+ sources
PTCH1(3), PTCH2(2)
0.400 1.000 5.06e-8 3.71e-7 ✓ sig. Cluster 203 →
Aniridia Anophthalmia
3 genes
Show details
3 of 3 corroborated by 2+ sources
ELP4(5), PAX6(4), SOX2(2)
0.143 0.333 5.01e-8 3.71e-7 ✓ sig. —
Atherosclerosis Lewy body disease
9 genes
Show details
8 of 9 corroborated by 2+ sources
APOC1(1), APOE(3), CLU(2), IGF2(2), AGER(2), SOD2(2), NOS2(2), EDN1(2), HRH1(3)
0.044 0.095 4.88e-8 3.63e-7 ✓ sig. —
Bone osteosarcoma Osteosarcoma
3 genes
Show details
3 of 3 corroborated by 2+ sources
CHEK2(3), TP53(3), RB1(3)
0.052 1.000 4.81e-8 3.58e-7 ✓ sig. Cluster 3 →
Auditory neuropathy Hereditary hearing loss
5 genes
Show details
5 of 5 corroborated by 2+ sources
OTOF(2), DIAPH1(2), MYO7A(2), WFS1(2), SLC17A8(2)
0.065 0.161 4.69e-8 3.49e-7 ✓ sig. Cluster 26 →
Cyclocephaly Semilobar holoprosencephaly
3 genes
Show details
3 of 3 corroborated by 2+ sources
FGF8(2), GAS1(2), ZIC2(2)
0.130 0.429 4.68e-8 3.48e-7 ✓ sig. —
Anorexia Nausea
3 genes
Show details
2 of 3 corroborated by 2+ sources
TNF(2), IFNA2(1), TNFRSF10A(2)
0.130 0.429 4.68e-8 3.48e-7 ✓ sig. —
Chorea Pemphigus vulgaris
3 genes
Show details
3 of 3 corroborated by 2+ sources
0.130 0.429 4.68e-8 3.48e-7 ✓ sig. Cluster 1 →
Congenital heart septal defect Congenital septal defect of heart
3 genes
Show details
3 of 3 corroborated by 2+ sources
PCSK5(2), NKX2-5(2), CITED2(2)
0.130 0.429 4.68e-8 3.48e-7 ✓ sig. —
Asbestosis Sepsis
4 genes
Show details
4 of 4 corroborated by 2+ sources
IL1B(2), TNF(2), NLRP3(2), NOS2(2)
0.083 0.235 4.62e-8 3.44e-7 ✓ sig. —
Cardiofaciocutaneous syndrome Myelomonocytic leukemia
3 genes
Show details
3 of 3 corroborated by 2+ sources
KRAS(8), NRAS(3), PTPN11(6)
0.150 0.300 4.33e-8 3.23e-7 ✓ sig. Cluster 42 →
Papilloma Tongue neoplasms
3 genes
Show details
SOD2(1), PTGS2(1), HRAS(1)
0.150 0.300 4.33e-8 3.23e-7 ✓ sig. Cluster 269 →
Cachexia Delirium
3 genes
Show details
3 of 3 corroborated by 2+ sources
IGF1(2), IL6(2), CXCL8(2)
0.150 0.300 4.33e-8 3.23e-7 ✓ sig. Cluster 76 →
Cachexia Esotropia
3 genes
Show details
2 of 3 corroborated by 2+ sources
TNF(2), PTGS2(2), CXCL8(1)
0.150 0.300 4.33e-8 3.23e-7 ✓ sig. Cluster 76 →

Showing 25 of 20813 pairs, sorted by significance (descending). Click a column header to sort.