Source: ALL
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: C0279658
Disease: Gallbladder squamous cell carcinoma
Gallbladder squamous cell carcinoma 		3 0 2 0.50 0 0
CUI: C1833693
Disease: Otodental Dysplasia
Otodental Dysplasia 		1 0 1 0.33 0 0
CUI: C1834013
Disease: Odontoma dysphagia syndrome
Odontoma dysphagia syndrome 		1 0 1 0.33 0 0
CUI: C4025862
Disease: Abnormality of the maxilla
Abnormality of the maxilla 		1 0 1 0.33 0 0
CUI: C0020627
Disease: Hypopharyngeal Neoplasms
Hypopharyngeal Neoplasms 		7 0 2 0.25 0 0
CUI: C0038368
Disease: Stomatognathic Diseases
Stomatognathic Diseases 		2 0 1 0.25 0 0
CUI: C0266604
Disease: Congenital aplasia of inner ear
Congenital aplasia of inner ear 		2 0 1 0.25 0 0
CUI: C0548923
Disease: Burn infection
Burn infection 		7 0 2 0.25 0 0
CUI: C1274228
Disease: Chylomicronemia syndrome
Chylomicronemia syndrome 		2 0 1 0.25 0 0
CUI: C2750325
Disease: Oculootodental syndrome
Oculootodental syndrome 		2 0 1 0.25 0 0
CUI: C3889891
Disease: APOLIPOPROTEIN C-II (PADOVA) PHENOTYPE
APOLIPOPROTEIN C-II (PADOVA) PHENOTYPE 		2 0 1 0.25 0 0
CUI: C4017134
Disease: APOLIPOPROTEIN C-II (PARIS) PHENOTYPE
APOLIPOPROTEIN C-II (PARIS) PHENOTYPE 		2 0 1 0.25 0 0
CUI: C4017135
Disease: APOLIPOPROTEIN C-II (BARI) PHENOTYPE
APOLIPOPROTEIN C-II (BARI) PHENOTYPE 		2 0 1 0.25 0 0
CUI: C4017136
Disease: APOLIPOPROTEIN C-II VARIANT PHENOTYPE
APOLIPOPROTEIN C-II VARIANT PHENOTYPE 		2 0 1 0.25 0 0
CUI: C4017137
Disease: APOLIPOPROTEIN C-II (SAN FRANCISCO)
APOLIPOPROTEIN C-II (SAN FRANCISCO) 		2 0 1 0.25 0 0
CUI: C4017138
Disease: apolipoprotein C-II (Wakayama) phenotype
apolipoprotein C-II (Wakayama) phenotype 		2 0 1 0.25 0 0
CUI: C4017139
Disease: APOLIPOPROTEIN C-II (AUCKLAND) PHENOTYPE
APOLIPOPROTEIN C-II (AUCKLAND) PHENOTYPE 		2 0 1 0.25 0 0
CUI: C4023566
Disease: Agenesis of premolar
Agenesis of premolar 		2 0 1 0.25 0 0
CUI: C0334050
Disease: Adenosis
Adenosis 		8 0 2 0.22 0 0
CUI: C0028882
Disease: Odontoma
Odontoma 		3 0 1 0.20 0 0
CUI: C1291447
Disease: Deficiency of triacylglycerol lipase
Deficiency of triacylglycerol lipase 		3 0 1 0.20 0 0
CUI: C1527284
Disease: Dental Pulp Stone
Dental Pulp Stone 		3 0 1 0.20 0 0
CUI: C1720779
Disease: Apolipoprotein C-II Deficiency (disorder)
Apolipoprotein C-II Deficiency (disorder) 		3 0 1 0.20 0 0
CUI: C1853144
Disease: Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia 		3 0 1 0.20 0 0
CUI: C4021175
Disease: Microtia, first degree
Microtia, first degree 		3 0 1 0.20 0 0