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: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis 		1 0 1 1.4E-02 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 1.4E-02 0 0
CUI: C0005146
Disease: Besnoitiasis
Besnoitiasis 		1 0 1 1.4E-02 0 0
CUI: C0006386
Disease: Bunion
Bunion 		1 0 1 1.4E-02 0 0
CUI: C0027095
Disease: Myosarcoma
Myosarcoma 		1 0 1 1.4E-02 0 0
CUI: C0037018
Disease: Shwartzman Phenomenon
Shwartzman Phenomenon 		1 0 1 1.4E-02 0 0
CUI: C0151731
Disease: Hepatic infarction
Hepatic infarction 		1 0 1 1.4E-02 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome 		1 0 1 1.4E-02 0 0
CUI: C0153053
Disease: Measles with complication
Measles with complication 		1 0 1 1.4E-02 0 0
CUI: C0155747
Disease: Aneurysm of splenic artery
Aneurysm of splenic artery 		1 0 1 1.4E-02 0 0
CUI: C0262509
Disease: herpetic neuralgia
herpetic neuralgia 		1 0 1 1.4E-02 0 0
CUI: C0262981
Disease: Interface dermatitis
Interface dermatitis 		1 0 1 1.4E-02 0 0
CUI: C0263506
Disease: Perifolliculitis capitis abscedens
Perifolliculitis capitis abscedens 		1 0 1 1.4E-02 0 0
CUI: C0263540
Disease: Nail Loss
Nail Loss 		1 0 1 1.4E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 1.4E-02 0 0
CUI: C0264356
Disease: Childhood bronchiectasis
Childhood bronchiectasis 		1 0 1 1.4E-02 0 0
CUI: C0268500
Disease: Yellow mutant oculocutaneous albinism
Yellow mutant oculocutaneous albinism 		1 0 1 1.4E-02 0 0
CUI: C0272328
Disease: Acquired factor X deficiency disease
Acquired factor X deficiency disease 		1 0 1 1.4E-02 0 0
CUI: C0272355
Disease: von Willebrand disease, type IIC
von Willebrand disease, type IIC 		1 0 1 1.4E-02 0 0
CUI: C0272356
Disease: von Willebrand disease, type IID
von Willebrand disease, type IID 		1 0 1 1.4E-02 0 0
CUI: C0275974
Disease: Glandular tularemia
Glandular tularemia 		1 0 1 1.4E-02 0 0
CUI: C0278716
Disease: recurrent Wilms tumor and other childhood kidney tumors
recurrent Wilms tumor and other childhood kidney tumors 		1 0 1 1.4E-02 0 0
CUI: C0332885
Disease: Congenital stenosis
Congenital stenosis 		1 0 1 1.4E-02 0 0
CUI: C0333008
Disease: Congenital hypopigmentation
Congenital hypopigmentation 		1 0 1 1.4E-02 0 0
CUI: C0333183
Disease: Partial stenosis
Partial stenosis 		1 0 1 1.4E-02 0 0