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: C4749271
Disease: Aleukemic mast cell leukemia
Aleukemic mast cell leukemia 		0 2 0 0 2 1.2E-03
CUI: C1303007
Disease: Brushfield spots
Brushfield spots 		14 0 1 1.2E-04 0 0
CUI: C2931092
Disease: Maternally Inherited Leigh Syndrome
Maternally Inherited Leigh Syndrome 		12 0 1 1.2E-04 0 0
CUI: C4022013
Disease: Multiple glomerular cysts
Multiple glomerular cysts 		12 0 1 1.2E-04 0 0
CUI: C4025585
Disease: Lacticaciduria
Lacticaciduria 		12 0 1 1.2E-04 0 0
CUI: C4551856
Disease: Asphyxiating Thoracic Dystrophy 1
Asphyxiating Thoracic Dystrophy 1 		11 0 1 1.2E-04 0 0
CUI: C0202159
Disease: Parathyroid hormone measurement
Parathyroid hormone measurement 		10 0 1 1.2E-04 0 0
CUI: C1845029
Disease: Nonprogressive cerebellar ataxia
Nonprogressive cerebellar ataxia 		9 0 1 1.2E-04 0 0
CUI: C1856655
Disease: Hypoplasia of olfactory tract
Hypoplasia of olfactory tract 		9 0 1 1.2E-04 0 0
CUI: C4022983
Disease: Abnormal ciliary motility
Abnormal ciliary motility 		9 0 1 1.2E-04 0 0
CUI: C1857332
Disease: Deafness, Sensorineural, Autosomal-Mitochondrial Type
Deafness, Sensorineural, Autosomal-Mitochondrial Type 		8 0 1 1.2E-04 0 0
CUI: C4022585
Disease: Fatigable weakness of distal limb muscles
Fatigable weakness of distal limb muscles 		8 0 1 1.2E-04 0 0
CUI: C4539789
Disease: Coiled sperm flagella
Coiled sperm flagella 		8 0 1 1.2E-04 0 0
CUI: C4757950
Disease: Isolated ATP synthase deficiency
Isolated ATP synthase deficiency 		8 0 1 1.2E-04 0 0
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome 		7 0 1 1.2E-04 0 0
CUI: C1837323
Disease: Decreased Achilles reflex
Decreased Achilles reflex 		7 0 1 1.2E-04 0 0
CUI: C1855923
Disease: Hyperphosphatasia with Mental Retardation
Hyperphosphatasia with Mental Retardation 		7 0 1 1.2E-04 0 0
CUI: C3665342
Disease: Progressive Cone Dystrophy
Progressive Cone Dystrophy 		7 0 1 1.2E-04 0 0
CUI: C3809221
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14 		7 0 1 1.2E-04 0 0
CUI: C4015184
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12 		7 0 1 1.2E-04 0 0
CUI: C4539786
Disease: Absent sperm flagella
Absent sperm flagella 		7 0 1 1.2E-04 0 0
CUI: C4539787
Disease: Short sperm flagella
Short sperm flagella 		7 0 1 1.2E-04 0 0
CUI: C0042790
Disease: Vision Disorders
Vision Disorders 		6 0 1 1.2E-04 0 0
CUI: C0233769
Disease: Micropsia
Micropsia 		6 0 1 1.2E-04 0 0
CUI: C0233771
Disease: Macropsia
Macropsia 		6 0 1 1.2E-04 0 0