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: C0036413
Disease: Scleredema Adultorum
Scleredema Adultorum 		1 0 1 5.9E-02 0 0
CUI: C0038557
Disease: Submandibular Gland Diseases
Submandibular Gland Diseases 		1 0 1 5.9E-02 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 5.9E-02 0 0
CUI: C0272328
Disease: Acquired factor X deficiency disease
Acquired factor X deficiency disease 		1 0 1 5.9E-02 0 0
CUI: C0272355
Disease: von Willebrand disease, type IIC
von Willebrand disease, type IIC 		1 0 1 5.9E-02 0 0
CUI: C0272356
Disease: von Willebrand disease, type IID
von Willebrand disease, type IID 		1 0 1 5.9E-02 0 0
CUI: C0276839
Disease: Infection by Cytauxzoon
Infection by Cytauxzoon 		1 0 1 5.9E-02 0 0
CUI: C0333183
Disease: Partial stenosis
Partial stenosis 		1 0 1 5.9E-02 0 0
CUI: C0339352
Disease: Capsular cataract (disorder)
Capsular cataract (disorder) 		1 0 1 5.9E-02 0 0
CUI: C0341022
Disease: Chronic hyperplastic candidiasis
Chronic hyperplastic candidiasis 		1 0 1 5.9E-02 0 0
CUI: C0343263
Disease: Chondrolysis of articular cartilage
Chondrolysis of articular cartilage 		1 0 1 5.9E-02 0 0
CUI: C0398610
Disease: Congenital von Willebrand's disease
Congenital von Willebrand's disease 		1 0 1 5.9E-02 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 5.9E-02 0 0
CUI: C0523633
Disease: Fibronectin measurement
Fibronectin measurement 		1 0 1 5.9E-02 0 0
CUI: C0598480
Disease: intestinal angiodysplasia
intestinal angiodysplasia 		1 0 1 5.9E-02 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 5.9E-02 0 0
CUI: C0795843
Disease: Chromosome 12 ring
Chromosome 12 ring 		1 0 1 5.9E-02 0 0
CUI: C0853856
Disease: Staphylococcal abscess
Staphylococcal abscess 		1 0 1 5.9E-02 0 0
CUI: C0865262
Disease: Thrombopathy
Thrombopathy 		1 0 1 5.9E-02 0 0
CUI: C0877456
Disease: Heyde's syndrome
Heyde's syndrome 		1 0 1 5.9E-02 0 0
CUI: C1842898
Disease: Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency 		1 0 1 5.9E-02 0 0
CUI: C1848108
Disease: Long ulna
Long ulna 		1 0 1 5.9E-02 0 0
CUI: C1848525
Disease: von Willebrand Disease, Recessive Form
von Willebrand Disease, Recessive Form 		1 0 1 5.9E-02 0 0
CUI: C1850671
Disease: Myosclerosis, Autosomal Recessive
Myosclerosis, Autosomal Recessive 		1 0 1 5.9E-02 0 0
CUI: C1855230
Disease: Focal lissencephaly
Focal lissencephaly 		1 0 1 5.9E-02 0 0