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: C1611706
Disease: Myosclerosis
Myosclerosis 		3 0 3 0.60 0 0
CUI: C1850851
Disease: Distal joint laxity
Distal joint laxity 		3 0 3 0.60 0 0
CUI: C4225636
Disease: ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1, AUTOSOMAL DOMINANT
ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1, AUTOSOMAL DOMINANT 		3 0 3 0.60 0 0
CUI: C1850855
Disease: Increased laxity of fingers
Increased laxity of fingers 		4 0 3 0.50 0 0
CUI: C1850853
Disease: Hyperextensibility at wrists
Hyperextensibility at wrists 		5 0 3 0.43 0 0
CUI: C4021054
Disease: Reduced muscle collagen VI
Reduced muscle collagen VI 		5 0 3 0.43 0 0
CUI: C1850848
Disease: Muscle fiber necrosis
Muscle fiber necrosis 		7 0 3 0.33 0 0
CUI: C4551860
Disease: Ullrich congenital muscular dystrophy
Ullrich congenital muscular dystrophy 		7 0 3 0.33 0 0
CUI: C0521532
Disease: Diaphragmatic paresis
Diaphragmatic paresis 		8 0 3 0.30 0 0
CUI: C4022161
Disease: Increased endomysial connective tissue
Increased endomysial connective tissue 		10 0 3 0.25 0 0
CUI: C0016512
Disease: Foot pain
Foot pain 		1 0 1 0.20 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta 		1 0 1 0.20 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula 		1 0 1 0.20 0 0
CUI: C1836485
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder) 		1 0 1 0.20 0 0
CUI: C1841686
Disease: Absent hallux
Absent hallux 		1 0 1 0.20 0 0
CUI: C1850671
Disease: Myosclerosis, Autosomal Recessive
Myosclerosis, Autosomal Recessive 		1 0 1 0.20 0 0
CUI: C1855003
Disease: Bilateral postaxial polydactyly
Bilateral postaxial polydactyly 		1 0 1 0.20 0 0
CUI: C1868111
Disease: Polydactyly, preaxial 4
Polydactyly, preaxial 4 		1 0 1 0.20 0 0
CUI: C1968943
Disease: Rudimentary to absent tibiae
Rudimentary to absent tibiae 		1 0 1 0.20 0 0
CUI: C2937300
Disease: Congenital hereditary muscular dystrophy
Congenital hereditary muscular dystrophy 		1 0 1 0.20 0 0
CUI: C3805692
Disease: Hyperpigmented nevi and streak
Hyperpigmented nevi and streak 		1 0 1 0.20 0 0
CUI: C4016298
Disease: POSTAXIAL POLYDACTYLY, TYPE A1/B
POSTAXIAL POLYDACTYLY, TYPE A1/B 		1 0 1 0.20 0 0
CUI: C4016299
Disease: GREIG CEPHALOPOLYSYNDACTYLY SYNDROME, SEVERE
GREIG CEPHALOPOLYSYNDACTYLY SYNDROME, SEVERE 		1 0 1 0.20 0 0
CUI: C4021235
Disease: 1-5 toe syndactyly
1-5 toe syndactyly 		1 0 1 0.20 0 0
CUI: C4022666
Disease: Partial absence of foot
Partial absence of foot 		1 0 1 0.20 0 0