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: C1853710
Disease: HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)
HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder) 		5 0 3 0.14 0 0
CUI: C0019816
Disease: Hereditary, Type VII, Motor and Sensory Neuropathy
Hereditary, Type VII, Motor and Sensory Neuropathy 		6 0 3 0.14 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot 		51 0 8 0.13 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment 		86 0 12 0.13 0 0
CUI: C1968790
Disease: Axonal degeneration/regeneration
Axonal degeneration/regeneration 		8 0 3 0.12 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe 		46 0 7 0.12 0 0
CUI: C0392553
Disease: Hereditary peripheral neuropathy
Hereditary peripheral neuropathy 		9 2 3 0.12 1 1.2E-02
CUI: C0270933
Disease: Inflammatory neuropathy
Inflammatory neuropathy 		19 0 4 0.12 0 0
CUI: C0728829
Disease: Congenital pes cavus
Congenital pes cavus 		19 15 4 0.12 2 2.1E-02
CUI: C0239830
Disease: Hand muscle atrophy
Hand muscle atrophy 		10 2 3 0.12 1 1.2E-02
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		70 0 9 0.11 0 0
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy 		95 14 11 0.11 3 3.2E-02
CUI: C0474520
Disease: Myokymia, Generalized
Myokymia, Generalized 		2 0 2 0.11 0 0
CUI: C0751922
Disease: Median Neuropathy
Median Neuropathy 		2 0 2 0.11 0 0
CUI: C1847896
Disease: Charcot-Marie-Tooth Disease, Dominant Intermediate A
Charcot-Marie-Tooth Disease, Dominant Intermediate A 		2 0 2 0.11 0 0
CUI: C1861675
Disease: Cold-induced muscle cramps
Cold-induced muscle cramps 		2 0 2 0.11 0 0
CUI: C2187547
Disease: Retroperitoneal Leiomyosarcoma
Retroperitoneal Leiomyosarcoma 		2 0 2 0.11 0 0
CUI: C4016264
Disease: DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT
DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT 		2 6 2 0.11 4 4.7E-02
CUI: C4518505
Disease: Partial trisomy of chromosome 17
Partial trisomy of chromosome 17 		2 0 2 0.11 0 0
CUI: C4721436
Disease: NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE
NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE 		2 4 2 0.11 3 3.5E-02
CUI: C0432185
Disease: Aplasia of muscle
Aplasia of muscle 		13 0 3 0.10 0 0
CUI: C1837552
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L (disorder) 		3 0 2 1.0E-01 0 0
CUI: C2750090
Disease: Charcot-Marie-Tooth Disease, Axonal, Type 2n
Charcot-Marie-Tooth Disease, Axonal, Type 2n 		3 0 2 1.0E-01 0 0
CUI: C4025132
Disease: Shortening of all distal phalanges of the toes
Shortening of all distal phalanges of the toes 		3 0 2 1.0E-01 0 0
CUI: C0270921
Disease: Axonal neuropathy
Axonal neuropathy 		59 0 7 9.9E-02 0 0