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 2.2E-02 0 0
CUI: C0040416
Disease: Tonic Pupil
Tonic Pupil 		1 0 1 2.2E-02 0 0
CUI: C0149662
Disease: Deformity of toe
Deformity of toe 		1 0 1 2.2E-02 0 0
CUI: C0234244
Disease: Tissue Pain
Tissue Pain 		1 0 1 2.2E-02 0 0
CUI: C0236960
Disease: Dementia due to Parkinson's disease
Dementia due to Parkinson's disease 		1 0 1 2.2E-02 0 0
CUI: C0264081
Disease: Osteoarthropathy of fingers familial
Osteoarthropathy of fingers familial 		1 0 1 2.2E-02 0 0
CUI: C0265280
Disease: Spondylometaphyseal dysplasia, Kozlowski type
Spondylometaphyseal dysplasia, Kozlowski type 		1 0 1 2.2E-02 0 0
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism 		1 0 1 2.2E-02 0 0
CUI: C0265573
Disease: Phocomelia of upper limb
Phocomelia of upper limb 		1 0 1 2.2E-02 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 2.2E-02 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 2.2E-02 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 2.2E-02 0 0
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I 		1 0 1 2.2E-02 0 0
CUI: C0282644
Disease: Smith-Lemli-Opitz Syndrome, Type II
Smith-Lemli-Opitz Syndrome, Type II 		1 0 1 2.2E-02 0 0
CUI: C0345286
Disease: Abnormal liver lobulation
Abnormal liver lobulation 		1 0 1 2.2E-02 0 0
CUI: C0422879
Disease: CNS symptom
CNS symptom 		1 0 1 2.2E-02 0 0
CUI: C0432227
Disease: Brachyolmia Type 3
Brachyolmia Type 3 		1 0 1 2.2E-02 0 0
CUI: C0456239
Disease: Peritoneal dialysis-associated peritonitis
Peritoneal dialysis-associated peritonitis 		1 0 1 2.2E-02 0 0
CUI: C0562557
Disease: Sexually disinhibited behavior
Sexually disinhibited behavior 		1 0 1 2.2E-02 0 0
CUI: C0585006
Disease: Deficiency of enoyl-CoA hydratase
Deficiency of enoyl-CoA hydratase 		1 0 1 2.2E-02 0 0
CUI: C0685732
Disease: Congenital dilatation of pulmonary artery
Congenital dilatation of pulmonary artery 		1 0 1 2.2E-02 0 0
CUI: C0751059
Disease: Cranial Neuropathies, Multiple
Cranial Neuropathies, Multiple 		1 0 1 2.2E-02 0 0
CUI: C0795865
Disease: Chromosome 17, trisomy 17p
Chromosome 17, trisomy 17p 		1 0 1 2.2E-02 0 0
CUI: C0850629
Disease: radiating back pain
radiating back pain 		1 0 1 2.2E-02 0 0
CUI: C0852085
Disease: Congenital connective tissue disorder
Congenital connective tissue disorder 		1 0 1 2.2E-02 0 0