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: C0936273
Disease: Familial Amyloid Polyneuropathy, Type IV
Familial Amyloid Polyneuropathy, Type IV 		2 0 2 0.25 0 0
CUI: C1719316
Disease: Inherited systemic amyloidosis
Inherited systemic amyloidosis 		2 0 2 0.25 0 0
CUI: C1628319
Disease: Lattice corneal dystrophy Type II
Lattice corneal dystrophy Type II 		4 0 2 0.20 0 0
CUI: C1851833
Disease: Premature birth following premature rupture of fetal membranes
Premature birth following premature rupture of fetal membranes 		5 0 2 0.18 0 0
CUI: C0010266
Disease: Cranial nerve diseases
Cranial nerve diseases 		7 0 2 0.15 0 0
CUI: C0155127
Disease: Familial Amyloid Polyneuropathy, Type V
Familial Amyloid Polyneuropathy, Type V 		8 0 2 0.14 0 0
CUI: C4024726
Disease: Mucopolysacchariduria
Mucopolysacchariduria 		8 0 2 0.14 0 0
CUI: C0268397
Disease: Amyloidosis, Primary Cutaneous
Amyloidosis, Primary Cutaneous 		9 0 2 0.13 0 0
CUI: C4543811
Disease: Adult-onset immunodeficiency
Adult-onset immunodeficiency 		9 0 2 0.13 0 0
CUI: C0016064
Disease: Fibrous Dysplasia, Monostotic
Fibrous Dysplasia, Monostotic 		1 0 1 0.12 0 0
CUI: C0033075
Disease: Presbyopia
Presbyopia 		1 0 1 0.12 0 0
CUI: C0201896
Disease: Arylsulfatase B measurement
Arylsulfatase B measurement 		1 0 1 0.12 0 0
CUI: C0241423
Disease: Atrophy of tongue
Atrophy of tongue 		10 0 2 0.12 0 0
CUI: C0265593
Disease: Brachymetacarpia
Brachymetacarpia 		1 0 1 0.12 0 0
CUI: C0268218
Disease: Maroteaux-Lamy syndrome, mild form
Maroteaux-Lamy syndrome, mild form 		1 0 1 0.12 0 0
CUI: C0268383
Disease: Familial amyloid polyneuropathy, type VI
Familial amyloid polyneuropathy, type VI 		1 0 1 0.12 0 0
CUI: C0268385
Disease: Familial Amyloid Polyneuropathy, Jewish Type
Familial Amyloid Polyneuropathy, Jewish Type 		1 0 1 0.12 0 0
CUI: C0268386
Disease: Amyloid Polyneuropathy, Swiss Type
Amyloid Polyneuropathy, Swiss Type 		1 0 1 0.12 0 0
CUI: C0281952
Disease: Pseudohypothyroidism
Pseudohypothyroidism 		1 0 1 0.12 0 0
CUI: C0339562
Disease: Amyloid of vitreous
Amyloid of vitreous 		1 0 1 0.12 0 0
CUI: C0342608
Disease: Amyloid Polyneuropathy, British Type (disorder)
Amyloid Polyneuropathy, British Type (disorder) 		1 0 1 0.12 0 0
CUI: C0423122
Disease: Ptosis of eyebrow
Ptosis of eyebrow 		1 0 1 0.12 0 0
CUI: C0546394
Disease: Nodular cutaneous amyloidosis
Nodular cutaneous amyloidosis 		1 0 1 0.12 0 0
CUI: C0700376
Disease: Pulmonary amyloidosis
Pulmonary amyloidosis 		1 0 1 0.12 0 0
CUI: C1527337
Disease: Familial Amyloid Polyneuropathy, Appalachian Type
Familial Amyloid Polyneuropathy, Appalachian Type 		1 0 1 0.12 0 0