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: C2931559
Disease: Chromosome 4q- Syndrome
Chromosome 4q- Syndrome 		1 0 1 0.50 0 0
CUI: C3553247
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 14
MENTAL RETARDATION, AUTOSOMAL DOMINANT 14 		1 0 1 0.50 0 0
CUI: C0265837
Disease: Congenital hypoplasia of tricuspid valve
Congenital hypoplasia of tricuspid valve 		2 0 1 0.33 0 0
CUI: C4020917
Disease: Absent fifth fingernail
Absent fifth fingernail 		2 0 1 0.33 0 0
CUI: C0474809
Disease: Endometrioid tumor
Endometrioid tumor 		3 0 1 0.25 0 0
CUI: C4021892
Disease: Absent fifth toenail
Absent fifth toenail 		3 0 1 0.25 0 0
CUI: C4289955
Disease: Atypical Endometriosis
Atypical Endometriosis 		3 0 1 0.25 0 0
CUI: C0030105
Disease: Ozena (disorder)
Ozena (disorder) 		4 0 1 0.20 0 0
CUI: C0265881
Disease: Congenital hypoplasia of aortic arch
Congenital hypoplasia of aortic arch 		4 0 1 0.20 0 0
CUI: C0678807
Disease: prenatal alcohol exposure
prenatal alcohol exposure 		5 0 1 0.17 0 0
CUI: C1848587
Disease: Isolated hypoplasia of the right ventricle
Isolated hypoplasia of the right ventricle 		5 0 1 0.17 0 0
CUI: C1861336
Disease: Aplasia/Hypoplasia of the distal phalanges of the hand
Aplasia/Hypoplasia of the distal phalanges of the hand 		6 0 1 0.14 0 0
CUI: C3277940
Disease: Generalized hypertrichosis
Generalized hypertrichosis 		6 0 1 0.14 0 0
CUI: C3281201
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 12
MENTAL RETARDATION, AUTOSOMAL DOMINANT 12 		6 0 1 0.14 0 0
CUI: C0007118
Disease: Carcinoma, Basosquamous
Carcinoma, Basosquamous 		7 0 1 0.12 0 0
CUI: C0271287
Disease: Schnyder crystalline corneal dystrophy
Schnyder crystalline corneal dystrophy 		7 0 1 0.12 0 0
CUI: C0334317
Disease: Cystadenofibroma
Cystadenofibroma 		8 0 1 0.11 0 0
CUI: C0344760
Disease: Congenital atresia of mitral valve
Congenital atresia of mitral valve 		8 0 1 0.11 0 0
CUI: C0279765
Disease: Endometrial Clear Cell Adenocarcinoma
Endometrial Clear Cell Adenocarcinoma 		10 0 1 9.1E-02 0 0
CUI: C4022120
Disease: Aplasia/Hypoplasia of the distal phalanx of the 5th toe
Aplasia/Hypoplasia of the distal phalanx of the 5th toe 		10 0 1 9.1E-02 0 0
CUI: C4024507
Disease: Aplasia/Hypoplasia of the distal phalanx of the 5th finger
Aplasia/Hypoplasia of the distal phalanx of the 5th finger 		10 0 1 9.1E-02 0 0
CUI: C0221287
Disease: Combined Hepatocellular Carcinoma and Cholangiocarcinoma
Combined Hepatocellular Carcinoma and Cholangiocarcinoma 		11 0 1 8.3E-02 0 0
CUI: C0272173
Disease: Myelokathexis
Myelokathexis 		11 0 1 8.3E-02 0 0
CUI: C4024682
Disease: Hypoplastic fifth fingernail
Hypoplastic fifth fingernail 		11 0 1 8.3E-02 0 0
CUI: C1836599
Disease: Macrocephaly at birth
Macrocephaly at birth 		12 0 1 7.7E-02 0 0