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: C0153614
Disease: Malignant neoplasm of ureteric orifice
Malignant neoplasm of ureteric orifice 		1 0 1 2.4E-02 0 0
CUI: C0234175
Disease: Palmar reflex
Palmar reflex 		1 0 1 2.4E-02 0 0
CUI: C0234244
Disease: Tissue Pain
Tissue Pain 		1 0 1 2.4E-02 0 0
CUI: C0234435
Disease: Syncope, Tussive
Syncope, Tussive 		1 0 1 2.4E-02 0 0
CUI: C0264081
Disease: Osteoarthropathy of fingers familial
Osteoarthropathy of fingers familial 		1 0 1 2.4E-02 0 0
CUI: C0264963
Disease: Aneurysm of femoral artery
Aneurysm of femoral artery 		1 0 1 2.4E-02 0 0
CUI: C0265280
Disease: Spondylometaphyseal dysplasia, Kozlowski type
Spondylometaphyseal dysplasia, Kozlowski type 		1 0 1 2.4E-02 0 0
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism 		1 0 1 2.4E-02 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta 		1 0 1 2.4E-02 0 0
CUI: C0266062
Disease: Posterior open bite
Posterior open bite 		1 0 1 2.4E-02 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula 		1 0 1 2.4E-02 0 0
CUI: C0270149
Disease: Perinatal respiratory distress
Perinatal respiratory distress 		1 0 1 2.4E-02 0 0
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I 		1 0 1 2.4E-02 0 0
CUI: C0282644
Disease: Smith-Lemli-Opitz Syndrome, Type II
Smith-Lemli-Opitz Syndrome, Type II 		1 0 1 2.4E-02 0 0
CUI: C0342826
Disease: 3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency 		1 0 1 2.4E-02 0 0
CUI: C0410654
Disease: Instability of atlantooccipital joint
Instability of atlantooccipital joint 		1 0 1 2.4E-02 0 0
CUI: C0423729
Disease: Chest pain on breathing
Chest pain on breathing 		1 0 1 2.4E-02 0 0
CUI: C0432227
Disease: Brachyolmia Type 3
Brachyolmia Type 3 		1 0 1 2.4E-02 0 0
CUI: C0562557
Disease: Sexually disinhibited behavior
Sexually disinhibited behavior 		1 0 1 2.4E-02 0 0
CUI: C0580550
Disease: Lymphocyte count abnormal
Lymphocyte count abnormal 		1 0 1 2.4E-02 0 0
CUI: C0749794
Disease: Upper Extremity Deformities, Congenital
Upper Extremity Deformities, Congenital 		1 0 1 2.4E-02 0 0
CUI: C0795821
Disease: Chromosome 7, trisomy 7q
Chromosome 7, trisomy 7q 		1 0 1 2.4E-02 0 0
CUI: C0796159
Disease: Mental retardation Smith Fineman Myers type
Mental retardation Smith Fineman Myers type 		1 0 1 2.4E-02 0 0
CUI: C1096121
Disease: Skeleton dysplasia
Skeleton dysplasia 		1 0 1 2.4E-02 0 0
CUI: C1112616
Disease: Loss of proprioception
Loss of proprioception 		1 0 1 2.4E-02 0 0