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: C0024967
Disease: Maximal Voluntary Ventilation
Maximal Voluntary Ventilation 		1 0 1 4.2E-02 0 0
CUI: C0153661
Disease: Malignant neoplasm of thorax
Malignant neoplasm of thorax 		1 0 1 4.2E-02 0 0
CUI: C0154863
Disease: Vitreoretinal dystrophy
Vitreoretinal dystrophy 		1 0 1 4.2E-02 0 0
CUI: C0519095
Disease: tuberculosis chronic pulmonary
tuberculosis chronic pulmonary 		1 0 1 4.2E-02 0 0
CUI: C1291610
Disease: Deficiency of mannose-6-phosphate isomerase
Deficiency of mannose-6-phosphate isomerase 		1 0 1 4.2E-02 0 0
CUI: C1842422
Disease: Synpolydactyly 2
Synpolydactyly 2 		1 0 1 4.2E-02 0 0
CUI: C1863416
Disease: Autosomal dominant compelling helio ophthalmic outburst syndrome
Autosomal dominant compelling helio ophthalmic outburst syndrome 		26 0 2 4.2E-02 0 0
CUI: C2751686
Disease: Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1
Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1 		1 0 1 4.2E-02 0 0
CUI: C3552634
Disease: LYMPHOPROLIFERATIVE SYNDROME 1
LYMPHOPROLIFERATIVE SYNDROME 1 		1 0 1 4.2E-02 0 0
CUI: C0239361
Disease: EXTREMITY MUSCLE ATROPHY, LOWER
EXTREMITY MUSCLE ATROPHY, LOWER 		2 0 1 4.0E-02 0 0
CUI: C0268687
Disease: Nutritional steatitis
Nutritional steatitis 		2 0 1 4.0E-02 0 0
CUI: C1442523
Disease: Enterostomy (morphologic abnormality)
Enterostomy (morphologic abnormality) 		2 0 1 4.0E-02 0 0
CUI: C4318844
Disease: Anaplastic sarcoma
Anaplastic sarcoma 		2 0 1 4.0E-02 0 0
CUI: C0016024
Disease: Fibroadenosis
Fibroadenosis 		3 0 1 3.8E-02 0 0
CUI: C1853255
Disease: Synpolydactyly 3
Synpolydactyly 3 		3 0 1 3.8E-02 0 0
CUI: C0014818
Disease: Erythroplasia
Erythroplasia 		4 0 1 3.7E-02 0 0
CUI: C1291601
Disease: Deficiency of isomerase
Deficiency of isomerase 		4 0 1 3.7E-02 0 0
CUI: C1853124
Disease: NEPHROTIC SYNDROME, TYPE 3
NEPHROTIC SYNDROME, TYPE 3 		4 0 1 3.7E-02 0 0
CUI: C1862697
Disease: Metatarsal synostosis
Metatarsal synostosis 		4 0 1 3.7E-02 0 0
CUI: C4283841
Disease: ITK Deficiency
ITK Deficiency 		4 0 1 3.7E-02 0 0
CUI: C1408258
Disease: Kidney damage
Kidney damage 		5 0 1 3.6E-02 0 0
CUI: C1865145
Disease: Congenital disorder of glycosylation type 1B
Congenital disorder of glycosylation type 1B 		5 0 1 3.6E-02 0 0
CUI: C0349571
Disease: Pleomorphic adenoma of parotid gland
Pleomorphic adenoma of parotid gland 		7 0 1 3.3E-02 0 0
CUI: C4317093
Disease: Reduced factor XI activity
Reduced factor XI activity 		7 0 1 3.3E-02 0 0
CUI: C0003463
Disease: Anus Neoplasms
Anus Neoplasms 		8 0 1 3.2E-02 0 0