Source: UNIPROT ×
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: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		4 6 2 0.22 1 2.2E-02
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		1 56 1 0.14 10 0.11
CUI: C0025268
Disease: Multiple Endocrine Neoplasia Type 2a
Multiple Endocrine Neoplasia Type 2a 		1 17 1 0.14 4 7.4E-02
CUI: C0025269
Disease: Multiple Endocrine Neoplasia Type 2b
Multiple Endocrine Neoplasia Type 2b 		1 0 1 0.14 0 0
CUI: C0030421
Disease: Paraganglioma
Paraganglioma 		1 6 1 0.14 2 4.4E-02
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		1 19 1 0.14 4 7.1E-02
CUI: C1837915
Disease: ERYTHROCYTOSIS, FAMILIAL, 2
ERYTHROCYTOSIS, FAMILIAL, 2 		1 6 1 0.14 1 2.2E-02
CUI: C1861848
Disease: PARAGANGLIOMAS 4
PARAGANGLIOMAS 4 		1 4 1 0.14 2 4.7E-02
CUI: C3150974
Disease: HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3 		1 4 1 0.14 1 2.3E-02
CUI: C3888239
Disease: HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 		1 33 1 0.14 1 1.4E-02
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
Transitional cell carcinoma of bladder 		3 0 1 0.11 0 0
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		3 0 1 0.11 0 0
CUI: C1855008
Disease: Mitochondrial Complex II Deficiency
Mitochondrial Complex II Deficiency 		3 0 1 0.11 0 0
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		7 0 1 7.7E-02 0 0
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		19 0 1 4.0E-02 0 0
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		54 0 1 1.7E-02 0 0
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		460 0 1 2.1E-03 0 0