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: C4225272
Disease: SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE 		1 0 1 0.11 0 0
CUI: C4225387
Disease: SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT
SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT 		1 0 1 0.11 0 0
CUI: C4225423
Disease: REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET
REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET 		1 0 1 0.11 0 0
CUI: C4310658
Disease: MYOCLONUS, INTRACTABLE, NEONATAL
MYOCLONUS, INTRACTABLE, NEONATAL 		1 0 1 0.11 0 0
CUI: C4310662
Disease: SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE 		1 0 1 0.11 0 0
CUI: C4551776
Disease: RITSCHER-SCHINZEL SYNDROME 1
RITSCHER-SCHINZEL SYNDROME 1 		1 0 1 0.11 0 0
CUI: C4693609
Disease: AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 25
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 25 		1 0 1 0.11 0 0
CUI: C4707173
Disease: Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation 		1 0 1 0.11 0 0
CUI: C4732774
Disease: Spastic paraparetic gait
Spastic paraparetic gait 		1 0 1 0.11 0 0
CUI: C4749335
Disease: Rippling muscle disease with myasthenia gravis
Rippling muscle disease with myasthenia gravis 		1 0 1 0.11 0 0
CUI: C4751434
Disease: Isolated asymptomatic elevation of creatine phosphokinase
Isolated asymptomatic elevation of creatine phosphokinase 		1 0 1 0.11 0 0
CUI: C0262918
Disease: Extraocular Muscle Paresis
Extraocular Muscle Paresis 		2 0 1 1.0E-01 0 0
CUI: C0268354
Disease: De Barsy syndrome
De Barsy syndrome 		2 0 1 1.0E-01 0 0
CUI: C0392477
Disease: Congenital flat foot
Congenital flat foot 		2 0 1 1.0E-01 0 0
CUI: C1112321
Disease: Congenital cutis laxa
Congenital cutis laxa 		2 0 1 1.0E-01 0 0
CUI: C1389102
Disease: Atrophy of the spinal cord
Atrophy of the spinal cord 		13 0 2 1.0E-01 0 0
CUI: C1832560
Disease: RIPPLING MUSCLE DISEASE 2 (disorder)
RIPPLING MUSCLE DISEASE 2 (disorder) 		2 0 1 1.0E-01 0 0
CUI: C1838254
Disease: RIPPLING MUSCLE DISEASE 1
RIPPLING MUSCLE DISEASE 1 		2 0 1 1.0E-01 0 0
CUI: C1846011
Disease: Pugilistic facies
Pugilistic facies 		2 0 1 1.0E-01 0 0
CUI: C1849115
Disease: SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder) 		2 0 1 1.0E-01 0 0
CUI: C1858106
Disease: SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT (disorder)
SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT (disorder) 		2 0 1 1.0E-01 0 0
CUI: C1863704
Disease: Spastic paraplegia 8, autosomal dominant
Spastic paraplegia 8, autosomal dominant 		2 0 1 1.0E-01 0 0
CUI: C2751987
Disease: Cutis Laxa, Autosomal Recessive, Type IIB
Cutis Laxa, Autosomal Recessive, Type IIB 		2 0 1 1.0E-01 0 0
CUI: C2931356
Disease: Spastic paraplegia type 5A, recessive
Spastic paraplegia type 5A, recessive 		13 0 2 1.0E-01 0 0
CUI: C3279093
Disease: LONG QT SYNDROME 2/9, DIGENIC
LONG QT SYNDROME 2/9, DIGENIC 		2 0 1 1.0E-01 0 0