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: C1300268
Disease: Brachydactyly syndrome type C
Brachydactyly syndrome type C 		2 0 1 7.1E-02 0 0
CUI: C1855091
Disease: Short proximal phalanx of thumb
Short proximal phalanx of thumb 		2 0 1 7.1E-02 0 0
CUI: C2750325
Disease: Oculootodental syndrome
Oculootodental syndrome 		2 0 1 7.1E-02 0 0
CUI: C3178892
Disease: Pelvic Floor Disorders
Pelvic Floor Disorders 		2 0 1 7.1E-02 0 0
CUI: C3264562
Disease: Buried penis
Buried penis 		2 0 1 7.1E-02 0 0
CUI: C4021438
Disease: Short distal phalanx of the 2nd finger
Short distal phalanx of the 2nd finger 		2 0 1 7.1E-02 0 0
CUI: C4021465
Disease: Pseudoepiphyses of the 2nd finger
Pseudoepiphyses of the 2nd finger 		2 0 1 7.1E-02 0 0
CUI: C4022107
Disease: Aplasia of the middle phalanges of the toes
Aplasia of the middle phalanges of the toes 		2 0 1 7.1E-02 0 0
CUI: C4022392
Disease: Early onset of sexual maturation
Early onset of sexual maturation 		2 0 1 7.1E-02 0 0
CUI: C4022580
Disease: Unfavorable response of muscle weakness to acetylcholine esterase inhibitors
Unfavorable response of muscle weakness to acetylcholine esterase inhibitors 		2 0 1 7.1E-02 0 0
CUI: C4024098
Disease: Aplasia/Hypoplasia of the 1st metacarpal
Aplasia/Hypoplasia of the 1st metacarpal 		2 0 1 7.1E-02 0 0
CUI: C4024235
Disease: Stippling of the epiphysis of the distal phalanx of the thumb
Stippling of the epiphysis of the distal phalanx of the thumb 		2 0 1 7.1E-02 0 0
CUI: C4039867
Disease: Acute hypoxemic respiratory failure
Acute hypoxemic respiratory failure 		2 0 1 7.1E-02 0 0
CUI: C4273756
Disease: Hepatoportal sclerosis
Hepatoportal sclerosis 		2 0 1 7.1E-02 0 0
CUI: C4722217
Disease: E-selectin Measurement
E-selectin Measurement 		2 0 1 7.1E-02 0 0
CUI: C0036347
Disease: Schizophrenia, Disorganized
Schizophrenia, Disorganized 		3 0 1 6.7E-02 0 0
CUI: C0221155
Disease: Systolic hypertension
Systolic hypertension 		19 0 2 6.7E-02 0 0
CUI: C0268350
Disease: Cutis Laxa, Autosomal Dominant
Cutis Laxa, Autosomal Dominant 		3 0 1 6.7E-02 0 0
CUI: C0406549
Disease: Cutis laxa, acquired type
Cutis laxa, acquired type 		3 0 1 6.7E-02 0 0
CUI: C0546389
Disease: Hepatic periportal necrosis
Hepatic periportal necrosis 		3 0 1 6.7E-02 0 0
CUI: C1698818
Disease: Photodamaged skin
Photodamaged skin 		3 0 1 6.7E-02 0 0
CUI: C1717804
Disease: Emphysema or COPD
Emphysema or COPD 		3 0 1 6.7E-02 0 0
CUI: C1856401
Disease: Glutaric Aciduria IIA
Glutaric Aciduria IIA 		3 0 1 6.7E-02 0 0
CUI: C1856403
Disease: Glutaric Aciduria IIB
Glutaric Aciduria IIB 		3 0 1 6.7E-02 0 0
CUI: C1856405
Disease: Glutaric Aciduria IIC
Glutaric Aciduria IIC 		3 0 1 6.7E-02 0 0