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: C0000821
Disease: Threatened abortion
Threatened abortion 		1 0 1 6.5E-03 0 0
CUI: C0001145
Disease: Acne Keloid
Acne Keloid 		1 0 1 6.5E-03 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 6.5E-03 0 0
CUI: C0023138
Disease: Laurence-Moon Syndrome
Laurence-Moon Syndrome 		1 0 1 6.5E-03 0 0
CUI: C0023441
Disease: Leukemia, Experimental
Leukemia, Experimental 		1 0 1 6.5E-03 0 0
CUI: C0024622
Disease: Malignant neoplasm of retina
Malignant neoplasm of retina 		1 0 1 6.5E-03 0 0
CUI: C0024950
Disease: Maxillary Diseases
Maxillary Diseases 		1 0 1 6.5E-03 0 0
CUI: C0024954
Disease: Maxillary Neoplasms
Maxillary Neoplasms 		1 0 1 6.5E-03 0 0
CUI: C0029437
Disease: Idiopathic Multicentric Osteolyses
Idiopathic Multicentric Osteolyses 		1 0 1 6.5E-03 0 0
CUI: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms 		1 0 1 6.5E-03 0 0
CUI: C0032357
Disease: Poland Syndrome
Poland Syndrome 		1 0 1 6.5E-03 0 0
CUI: C0037050
Disease: Sick Building Syndrome
Sick Building Syndrome 		1 0 1 6.5E-03 0 0
CUI: C0042818
Disease: Visual discomfort
Visual discomfort 		1 0 1 6.5E-03 0 0
CUI: C0085438
Disease: Meningitis, Fungal
Meningitis, Fungal 		1 0 1 6.5E-03 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome 		1 0 1 6.5E-03 0 0
CUI: C0153470
Disease: Malignant neoplasm of spleen
Malignant neoplasm of spleen 		1 0 1 6.5E-03 0 0
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea 		1 0 1 6.5E-03 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 6.5E-03 0 0
CUI: C0221360
Disease: Congenital absence of diaphragm
Congenital absence of diaphragm 		1 0 1 6.5E-03 0 0
CUI: C0240583
Disease: Short upturned nose
Short upturned nose 		1 0 1 6.5E-03 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 6.5E-03 0 0
CUI: C0264402
Disease: Gas bubble disease
Gas bubble disease 		1 0 1 6.5E-03 0 0
CUI: C0264954
Disease: Arteriovascular degeneration
Arteriovascular degeneration 		1 0 1 6.5E-03 0 0
CUI: C0265241
Disease: Franceschetti-Klein syndrome
Franceschetti-Klein syndrome 		1 0 1 6.5E-03 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 6.5E-03 0 0