Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C4324434
Disease: Panniculus
Panniculus
4 0 2 0.33 0 0
CUI: C4087491
Disease: End stage COPD
End stage COPD
5 0 2 0.29 0 0
CUI: C0025211
Disease: Conjunctival melanosis
Conjunctival melanosis
1 0 1 0.25 0 0
CUI: C0332877
Disease: Congenital premature fusion
Congenital premature fusion
6 0 2 0.25 0 0
CUI: C0340639
Disease: Carotid artery aneurysm
Carotid artery aneurysm
1 0 1 0.25 0 0
CUI: C0524686
Disease: Periodontitis, Acute Nonsuppurative
Periodontitis, Acute Nonsuppurative
1 0 1 0.25 0 0
CUI: C0542142
Disease: Recurrent Laryngeal Nerve Paralysis
Recurrent Laryngeal Nerve Paralysis
1 0 1 0.25 0 0
CUI: C1266176
Disease: Atypical choroid plexus papilloma
Atypical choroid plexus papilloma
1 0 1 0.25 0 0
CUI: C1333100
Disease: Squamous cell carcinoma of colon
Squamous cell carcinoma of colon
1 0 1 0.25 0 0
CUI: C1333987
Disease: Hereditary Glomangioma
Hereditary Glomangioma
1 0 1 0.25 0 0
CUI: C1334687
Disease: Megakaryocytic Neoplasm
Megakaryocytic Neoplasm
1 0 1 0.25 0 0
CUI: C4087190
Disease: Sulcus vocalis
Sulcus vocalis
1 0 1 0.25 0 0
CUI: C0040262
Disease: Tinea Versicolor
Tinea Versicolor
2 0 1 0.20 0 0
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome
8 0 2 0.20 0 0
CUI: C0410334
Disease: Defect of articular cartilage
Defect of articular cartilage
2 0 1 0.20 0 0
Signet-ring cell adenocarcinoma gastric
8 0 2 0.20 0 0
CUI: C1562893
Disease: Retrocorneal fibrous membrane
Retrocorneal fibrous membrane
2 0 1 0.20 0 0
CUI: C1835895
Disease: RETINITIS PIGMENTOSA 33 (disorder)
RETINITIS PIGMENTOSA 33 (disorder)
2 0 1 0.20 0 0
Optic Nerve Hypoplasia and Abnormalities of the Central Nervous System
2 0 1 0.20 0 0
CUI: C0008298
Disease: Polyp in nasopharynx
Polyp in nasopharynx
3 0 1 0.17 0 0
CUI: C0039981
Disease: Thoracic Neoplasms
Thoracic Neoplasms
3 0 1 0.17 0 0
CUI: C0334473
Disease: Intramuscular lipoma
Intramuscular lipoma
3 0 1 0.17 0 0
CUI: C0701824
Disease: Staggering gait
Staggering gait
3 0 1 0.17 0 0
CUI: C3281247
Disease: BENT BONE DYSPLASIA SYNDROME
BENT BONE DYSPLASIA SYNDROME
3 0 1 0.17 0 0
CUI: C1300257
Disease: Thanatophoric dysplasia, type 2
Thanatophoric dysplasia, type 2
11 0 2 0.15 0 0