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: C0852262
Disease: Placental abnormalities (excl neoplasms)
Placental abnormalities (excl neoplasms) 		12 0 1 8.3E-02 0 0
CUI: C0008767
Disease: Cicatrization
Cicatrization 		13 0 1 7.7E-02 0 0
CUI: C1389102
Disease: Atrophy of the spinal cord
Atrophy of the spinal cord 		13 0 1 7.7E-02 0 0
CUI: C3806301
Disease: Scarring alopecia of scalp
Scarring alopecia of scalp 		13 0 1 7.7E-02 0 0
CUI: C0239831
Disease: Hand muscle weakness
Hand muscle weakness 		14 0 1 7.1E-02 0 0
CUI: C2932678
Disease: Inherited Peripheral Neuropathy
Inherited Peripheral Neuropathy 		14 0 1 7.1E-02 0 0
CUI: C3276549
Disease: OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY
OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY 		14 0 1 7.1E-02 0 0
CUI: C0240914
Disease: Romberg's sign positive
Romberg's sign positive 		15 0 1 6.7E-02 0 0
CUI: C0577655
Disease: Quadriceps weakness
Quadriceps weakness 		15 0 1 6.7E-02 0 0
CUI: C0023801
Disease: Lipomatosis
Lipomatosis 		16 0 1 6.2E-02 0 0
CUI: C0574769
Disease: Loss of scalp hair
Loss of scalp hair 		16 0 1 6.2E-02 0 0
CUI: C0677050
Disease: Manganese Poisoning
Manganese Poisoning 		16 0 1 6.2E-02 0 0
CUI: C4551508
Disease: Dominant hereditary optic atrophy
Dominant hereditary optic atrophy 		16 0 1 6.2E-02 0 0
CUI: C1836392
Disease: Dysmetric saccades
Dysmetric saccades 		18 0 1 5.6E-02 0 0
CUI: C2230441
Disease: Triceps weakness
Triceps weakness 		18 0 1 5.6E-02 0 0
CUI: C4025614
Disease: EMG: chronic denervation signs
EMG: chronic denervation signs 		18 0 1 5.6E-02 0 0
CUI: C0745287
Disease: infertility tubal factor
infertility tubal factor 		19 0 1 5.3E-02 0 0
CUI: C0600520
Disease: Left Ventricle Remodeling
Left Ventricle Remodeling 		21 0 1 4.8E-02 0 0
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy 		21 0 1 4.8E-02 0 0
CUI: C1408182
Disease: Hereditary motor and sensory neuropathy, types I-IV
Hereditary motor and sensory neuropathy, types I-IV 		21 0 1 4.8E-02 0 0
CUI: C2875300
Disease: Peroneal muscular atrophy (axonal type) (hypertrophic type)
Peroneal muscular atrophy (axonal type) (hypertrophic type) 		21 0 1 4.8E-02 0 0
CUI: C1844806
Disease: Weight less than 3rd percentile
Weight less than 3rd percentile 		22 0 1 4.5E-02 0 0
CUI: C1854919
Disease: Severe psychomotor retardation
Severe psychomotor retardation 		22 3 1 4.5E-02 1 8.3E-02
CUI: C0393814
Disease: Hereditary liability to pressure palsies
Hereditary liability to pressure palsies 		23 0 1 4.3E-02 0 0
CUI: C1842587
Disease: Sensory axonal neuropathy
Sensory axonal neuropathy 		23 0 1 4.3E-02 0 0