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: C0152200
Disease: Achromatopsia
Achromatopsia 		26 63 6 0.11 1 1.5E-02
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis 		17 0 5 0.11 0 0
CUI: C4733333
Disease: familial non-medullary thyroid cancer
familial non-medullary thyroid cancer 		17 0 5 0.11 0 0
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		29 0 6 0.11 0 0
CUI: C3887980
Disease: Protanomaly
Protanomaly 		19 0 5 0.11 0 0
CUI: C0036211
Disease: Sarcoma 180
Sarcoma 180 		20 0 5 0.10 0 0
CUI: C0302129
Disease: Achromatopsia 1
Achromatopsia 1 		20 0 5 0.10 0 0
CUI: C0311361
Disease: Adenomatous goiter
Adenomatous goiter 		23 0 5 9.8E-02 0 0
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias 		83 0 10 9.4E-02 0 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy 		25 0 5 9.4E-02 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 0 5 9.4E-02 0 0
CUI: C4076240
Disease: Chronic kidney disease mineral and bone disorder
Chronic kidney disease mineral and bone disorder 		26 0 5 9.3E-02 0 0
CUI: C0030472
Disease: Paraneoplastic Syndromes
Paraneoplastic Syndromes 		28 0 5 8.9E-02 0 0
CUI: C0497550
Disease: Benign neurologic neoplasms
Benign neurologic neoplasms 		29 0 5 8.8E-02 0 0
CUI: C0029134
Disease: Optic Neuritis
Optic Neuritis 		79 0 9 8.7E-02 0 0
CUI: C2825306
Disease: Treatment related leukaemia
Treatment related leukaemia 		30 0 5 8.6E-02 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		43 0 6 8.6E-02 0 0
CUI: C0035934
Disease: Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome 		31 0 5 8.5E-02 0 0
CUI: C0346398
Disease: Mixed follicular and papillary thyroid carcinoma
Mixed follicular and papillary thyroid carcinoma 		31 0 5 8.5E-02 0 0
CUI: C3896673
Disease: Familial Nonmedullary Thyroid Gland Carcinoma
Familial Nonmedullary Thyroid Gland Carcinoma 		31 0 5 8.5E-02 0 0
CUI: C1262037
Disease: Diabetic cystopathy
Diabetic cystopathy 		6 0 3 8.3E-02 0 0
CUI: C3665342
Disease: Progressive Cone Dystrophy
Progressive Cone Dystrophy 		7 0 3 8.1E-02 0 0
CUI: C0032339
Disease: Rothmund-Thomson syndrome
Rothmund-Thomson syndrome 		35 0 5 7.9E-02 0 0
CUI: C0342190
Disease: C-cell hyperplasia of thyroid
C-cell hyperplasia of thyroid 		35 0 5 7.9E-02 0 0
CUI: C3831784
Disease: Acute monocytic/monoblastic leukemia
Acute monocytic/monoblastic leukemia 		35 0 5 7.9E-02 0 0