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: C4022674
Disease: Auricular tag
Auricular tag 		1 0 1 0.20 0 0
CUI: C4023586
Disease: Aplasia/Hypoplasia of the vagina
Aplasia/Hypoplasia of the vagina 		1 0 1 0.20 0 0
CUI: C4024086
Disease: Aplasia of the 4th metacarpal
Aplasia of the 4th metacarpal 		1 0 1 0.20 0 0
CUI: C4024090
Disease: Aplasia of the 2nd metacarpal
Aplasia of the 2nd metacarpal 		1 0 1 0.20 0 0
CUI: C4024136
Disease: Polydactyly affecting the 4th finger
Polydactyly affecting the 4th finger 		1 0 1 0.20 0 0
CUI: C4024144
Disease: Polydactyly affecting the 3rd finger
Polydactyly affecting the 3rd finger 		1 0 1 0.20 0 0
CUI: C4024634
Disease: Distal urethral duplication
Distal urethral duplication 		1 0 1 0.20 0 0
CUI: C4025113
Disease: Proximal tibial and fibular fusion
Proximal tibial and fibular fusion 		1 0 1 0.20 0 0
CUI: C4025153
Disease: Dysplastic distal thumb phalanges with a central hole
Dysplastic distal thumb phalanges with a central hole 		1 0 1 0.20 0 0
CUI: C4025774
Disease: 1-3 toe syndactyly
1-3 toe syndactyly 		1 0 1 0.20 0 0
CUI: C4225336
Disease: DYSTONIA 27
DYSTONIA 27 		1 0 1 0.20 0 0
CUI: C4225638
Disease: BETHLEM MYOPATHY 1, AUTOSOMAL RECESSIVE
BETHLEM MYOPATHY 1, AUTOSOMAL RECESSIVE 		1 0 1 0.20 0 0
CUI: C4310725
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B 		1 0 1 0.20 0 0
CUI: C4310875
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2A
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2A 		1 0 1 0.20 0 0
CUI: C4707897
Disease: Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
Severe early-onset axonal neuropathy due to mitofusin 2 deficiency 		1 0 1 0.20 0 0
CUI: C4721887
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A 		1 0 1 0.20 0 0
CUI: C1843643
Disease: Nocturnal hypoventilation
Nocturnal hypoventilation 		14 0 3 0.19 0 0
CUI: C0013570
Disease: Ecthyma, Contagious
Ecthyma, Contagious 		2 0 1 0.17 0 0
CUI: C0263445
Disease: Acne fulminans
Acne fulminans 		2 0 1 0.17 0 0
CUI: C0545617
Disease: Supernumerary metacarpal bone
Supernumerary metacarpal bone 		2 0 1 0.17 0 0
CUI: C1840310
Disease: Midline facial capillary hemangioma
Midline facial capillary hemangioma 		2 0 1 0.17 0 0
CUI: C4021333
Disease: Mesoaxial foot polydactyly
Mesoaxial foot polydactyly 		2 0 1 0.17 0 0
CUI: C4021663
Disease: Abnormality of muscle fibers
Abnormality of muscle fibers 		2 0 1 0.17 0 0
CUI: C4048262
Disease: Hydronephrosis Due To Pujo
Hydronephrosis Due To Pujo 		2 0 1 0.17 0 0
CUI: C0410179
Disease: Ullrich congenital muscular dystrophy 1
Ullrich congenital muscular dystrophy 1 		17 0 3 0.16 0 0