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: C4310807
Disease: BRACHYDACTYLY-SYNDACTYLY-OLIGODACTYLY SYNDROME
BRACHYDACTYLY-SYNDACTYLY-OLIGODACTYLY SYNDROME 		1 0 1 6.7E-02 0 0
CUI: C4512053
Disease: 4p16.3 microduplication syndrome
4p16.3 microduplication syndrome 		1 0 1 6.7E-02 0 0
CUI: C4520921
Disease: Stage 0 Gastric Cancer AJCC v6 and v7
Stage 0 Gastric Cancer AJCC v6 and v7 		1 0 1 6.7E-02 0 0
CUI: C4553656
Disease: Rectal Stenosis, CTCAE
Rectal Stenosis, CTCAE 		1 0 1 6.7E-02 0 0
CUI: C4707448
Disease: Ring chromosome 2 syndrome
Ring chromosome 2 syndrome 		1 0 1 6.7E-02 0 0
CUI: C0158662
Disease: Congenital anomaly of tongue
Congenital anomaly of tongue 		2 0 1 6.2E-02 0 0
CUI: C0235956
Disease: Absence attacks
Absence attacks 		2 0 1 6.2E-02 0 0
CUI: C0265312
Disease: Brachydactyly syndrome type E
Brachydactyly syndrome type E 		2 0 1 6.2E-02 0 0
CUI: C0265581
Disease: Longitudinal deficiency of radius
Longitudinal deficiency of radius 		2 0 1 6.2E-02 0 0
CUI: C0265931
Disease: Persistent left superior vena cava
Persistent left superior vena cava 		2 0 1 6.2E-02 0 0
CUI: C0266981
Disease: Torus palatinus
Torus palatinus 		2 0 1 6.2E-02 0 0
CUI: C0278769
Disease: Chronic lymphocytic leukaemia stage 3
Chronic lymphocytic leukaemia stage 3 		2 0 1 6.2E-02 0 0
CUI: C0302246
Disease: Hexadactyly
Hexadactyly 		2 0 1 6.2E-02 0 0
CUI: C0431415
Disease: Lumbosacral agenesis
Lumbosacral agenesis 		2 0 1 6.2E-02 0 0
CUI: C0431943
Disease: Lower Extremity Deformities, Congenital
Lower Extremity Deformities, Congenital 		2 0 1 6.2E-02 0 0
CUI: C0795805
Disease: Chromosome 2, trisomy 2q
Chromosome 2, trisomy 2q 		2 0 1 6.2E-02 0 0
CUI: C1290800
Disease: Acquired anomaly of tongue
Acquired anomaly of tongue 		2 0 1 6.2E-02 0 0
CUI: C1332582
Disease: Primary bone lymphoma
Primary bone lymphoma 		2 0 1 6.2E-02 0 0
CUI: C1710501
Disease: Pleuropulmonary blastoma type I
Pleuropulmonary blastoma type I 		2 0 1 6.2E-02 0 0
CUI: C1836861
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP I
FANCONI ANEMIA, COMPLEMENTATION GROUP I 		2 0 1 6.2E-02 0 0
CUI: C1838568
Disease: Sacral defect and anterior sacral meningocele
Sacral defect and anterior sacral meningocele 		2 0 1 6.2E-02 0 0
CUI: C1838569
Disease: Caudal Dysgenesis Syndrome
Caudal Dysgenesis Syndrome 		2 0 1 6.2E-02 0 0
CUI: C1842464
Disease: Nablus mask-like facial syndrome
Nablus mask-like facial syndrome 		2 0 1 6.2E-02 0 0
CUI: C1853137
Disease: BRACHYDACTYLY-SYNDACTYLY SYNDROME
BRACHYDACTYLY-SYNDACTYLY SYNDROME 		2 0 1 6.2E-02 0 0
CUI: C1856892
Disease: Facial Dysmorphism with Multiple Malformations
Facial Dysmorphism with Multiple Malformations 		2 0 1 6.2E-02 0 0