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: C1968790
Disease: Axonal degeneration/regeneration
Axonal degeneration/regeneration 		8 0 2 6.5E-02 0 0
CUI: C2936797
Disease: Acid cholesteryl ester hydrolase deficiency, type 2
Acid cholesteryl ester hydrolase deficiency, type 2 		9 0 2 6.2E-02 0 0
CUI: C3551426
Disease: Dystrophic fingernails
Dystrophic fingernails 		27 0 3 6.1E-02 0 0
CUI: C0025164
Disease: Megaesophagus
Megaesophagus 		10 0 2 6.1E-02 0 0
CUI: C3274592
Disease: Lipofibromatosis
Lipofibromatosis 		11 0 2 5.9E-02 0 0
CUI: C0029443
Disease: Osteomyelitis
Osteomyelitis 		121 0 8 5.8E-02 0 0
CUI: C0020620
Disease: Hypohidrosis
Hypohidrosis 		69 0 5 5.6E-02 0 0
CUI: C4021816
Disease: Abnormality of the gingiva
Abnormality of the gingiva 		13 0 2 5.6E-02 0 0
CUI: C0027888
Disease: Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathies 		53 0 4 5.4E-02 0 0
CUI: C1859606
Disease: Decreased number of large peripheral myelinated nerve fibers
Decreased number of large peripheral myelinated nerve fibers 		14 0 2 5.4E-02 0 0
CUI: C2932678
Disease: Inherited Peripheral Neuropathy
Inherited Peripheral Neuropathy 		14 0 2 5.4E-02 0 0
CUI: C0155119
Disease: Recurrent erosion of cornea
Recurrent erosion of cornea 		15 0 2 5.3E-02 0 0
CUI: C0240914
Disease: Romberg's sign positive
Romberg's sign positive 		15 0 2 5.3E-02 0 0
CUI: C0038870
Disease: Neuralgia, Supraorbital
Neuralgia, Supraorbital 		16 0 2 5.1E-02 0 0
CUI: C0042656
Disease: Neuralgia, Vidian
Neuralgia, Vidian 		16 0 2 5.1E-02 0 0
CUI: C0234247
Disease: Neuralgia, Atypical
Neuralgia, Atypical 		16 0 2 5.1E-02 0 0
CUI: C0234249
Disease: Neuralgia, Stump
Neuralgia, Stump 		16 0 2 5.1E-02 0 0
CUI: C0344505
Disease: Alacrima
Alacrima 		16 0 2 5.1E-02 0 0
CUI: C0423711
Disease: Neuralgia, Perineal
Neuralgia, Perineal 		16 0 2 5.1E-02 0 0
CUI: C0423712
Disease: Neuralgia, Iliohypogastric Nerve
Neuralgia, Iliohypogastric Nerve 		16 0 2 5.1E-02 0 0
CUI: C0751371
Disease: Neuralgia, Ilioinguinal
Neuralgia, Ilioinguinal 		16 0 2 5.1E-02 0 0
CUI: C0751373
Disease: Paroxysmal Nerve Pain
Paroxysmal Nerve Pain 		16 0 2 5.1E-02 0 0
CUI: C0423318
Disease: Heterochromia iridis
Heterochromia iridis 		17 0 2 5.0E-02 0 0
CUI: C0432284
Disease: Infantile myofibromatosis
Infantile myofibromatosis 		18 0 2 4.9E-02 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies 		104 0 6 4.9E-02 0 0