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: C3278204
Disease: Dysmyelinating leukodystrophy
Dysmyelinating leukodystrophy 		4 2 2 0.25 2 0.50
CUI: C0400973
Disease: Synthetic defect of bile acids
Synthetic defect of bile acids 		1 0 1 0.17 0 0
CUI: C0555197
Disease: Florid cemento-osseous dysplasia
Florid cemento-osseous dysplasia 		1 0 1 0.17 0 0
CUI: C1969785
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder) 		1 0 1 0.17 0 0
CUI: C3495361
Disease: Gigantiform Cementoma, Familial
Gigantiform Cementoma, Familial 		1 0 1 0.17 0 0
CUI: C3806702
Disease: CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6
CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6 		1 0 1 0.17 0 0
CUI: C4022148
Disease: Abnormality of the dentate nucleus
Abnormality of the dentate nucleus 		1 0 1 0.17 0 0
CUI: C4022163
Disease: Abnormality of central somatosensory evoked potentials
Abnormality of central somatosensory evoked potentials 		1 0 1 0.17 0 0
CUI: C4310662
Disease: SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE 		1 0 1 0.17 0 0
CUI: C4706411
Disease: X-linked Charcot-Marie-Tooth disease type 6
X-linked Charcot-Marie-Tooth disease type 6 		1 0 1 0.17 0 0
CUI: C0268252
Disease: Late-Onset Globoid Cell Leukodystrophy
Late-Onset Globoid Cell Leukodystrophy 		2 0 1 0.14 0 0
CUI: C0586738
Disease: Calf muscle weakness
Calf muscle weakness 		2 0 1 0.14 0 0
CUI: C0751273
Disease: Infantile Globoid Cell Leukodystrophy
Infantile Globoid Cell Leukodystrophy 		2 0 1 0.14 0 0
CUI: C1833739
Disease: Diaphyseal cortical sclerosis
Diaphyseal cortical sclerosis 		2 0 1 0.14 0 0
CUI: C1969722
Disease: Impaired pursuit initiation and maintenance
Impaired pursuit initiation and maintenance 		2 0 1 0.14 0 0
CUI: C2673266
Disease: KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY
KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY 		2 0 1 0.14 0 0
CUI: C2750076
Disease: Miyoshi Muscular Dystrophy 3
Miyoshi Muscular Dystrophy 3 		2 0 1 0.14 0 0
CUI: C3809008
Disease: HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEG SPASTICITY
HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEG SPASTICITY 		2 0 1 0.14 0 0
CUI: C4023376
Disease: Abnormality of the dorsal column of the spinal cord
Abnormality of the dorsal column of the spinal cord 		2 0 1 0.14 0 0
CUI: C4024772
Disease: Abnormal flash visual evoked potentials
Abnormal flash visual evoked potentials 		2 0 1 0.14 0 0
CUI: C0011103
Disease: Decerebrate State
Decerebrate State 		3 0 1 0.12 0 0
CUI: C1112261
Disease: Gaze palsy
Gaze palsy 		3 0 1 0.12 0 0
CUI: C1290708
Disease: Osteomyelitis of mandible
Osteomyelitis of mandible 		3 0 1 0.12 0 0
CUI: C1522133
Disease: Hypercholesterolemia result
Hypercholesterolemia result 		3 0 1 0.12 0 0
CUI: C4024603
Disease: Atrophy of quadriceps femoris muscle
Atrophy of quadriceps femoris muscle 		3 0 1 0.12 0 0