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: C0016512
Disease: Foot pain
Foot pain 		1 0 1 3.8E-02 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 3.8E-02 0 0
CUI: C0040416
Disease: Tonic Pupil
Tonic Pupil 		1 0 1 3.8E-02 0 0
CUI: C0234244
Disease: Tissue Pain
Tissue Pain 		1 0 1 3.8E-02 0 0
CUI: C0235198
Disease: Unable to concentrate
Unable to concentrate 		1 0 1 3.8E-02 0 0
CUI: C0236960
Disease: Dementia due to Parkinson's disease
Dementia due to Parkinson's disease 		1 0 1 3.8E-02 0 0
CUI: C0264081
Disease: Osteoarthropathy of fingers familial
Osteoarthropathy of fingers familial 		1 0 1 3.8E-02 0 0
CUI: C0265280
Disease: Spondylometaphyseal dysplasia, Kozlowski type
Spondylometaphyseal dysplasia, Kozlowski type 		1 0 1 3.8E-02 0 0
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism 		1 0 1 3.8E-02 0 0
CUI: C0333072
Disease: Claw-shaped deformity
Claw-shaped deformity 		1 0 1 3.8E-02 0 0
CUI: C0422879
Disease: CNS symptom
CNS symptom 		1 0 1 3.8E-02 0 0
CUI: C0432227
Disease: Brachyolmia Type 3
Brachyolmia Type 3 		1 0 1 3.8E-02 0 0
CUI: C0562557
Disease: Sexually disinhibited behavior
Sexually disinhibited behavior 		1 0 1 3.8E-02 0 0
CUI: C0751059
Disease: Cranial Neuropathies, Multiple
Cranial Neuropathies, Multiple 		1 0 1 3.8E-02 0 0
CUI: C0795865
Disease: Chromosome 17, trisomy 17p
Chromosome 17, trisomy 17p 		1 0 1 3.8E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 3.8E-02 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 3.8E-02 0 0
CUI: C0850629
Disease: radiating back pain
radiating back pain 		1 0 1 3.8E-02 0 0
CUI: C1695985
Disease: Lewis-Sumner syndrome
Lewis-Sumner syndrome 		1 0 1 3.8E-02 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 3.8E-02 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 3.8E-02 0 0
CUI: C1836336
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H 		1 0 1 3.8E-02 0 0
CUI: C1836485
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder) 		1 0 1 3.8E-02 0 0
CUI: C1837805
Disease: Charcot-Marie-Tooth disease, axonal, Type 2G
Charcot-Marie-Tooth disease, axonal, Type 2G 		1 0 1 3.8E-02 0 0
CUI: C1838492
Disease: SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder)
SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder) 		1 0 1 3.8E-02 0 0