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: C0393590
Disease: Fahr's syndrome (disorder)
Fahr's syndrome (disorder) 		10 0 5 0.24 0 0
CUI: C4324314
Disease: Primary familial brain calcification
Primary familial brain calcification 		12 0 5 0.22 0 0
CUI: C1859273
Disease: Dense calcifications in the cerebellar dentate nucleus
Dense calcifications in the cerebellar dentate nucleus 		3 0 3 0.19 0 0
CUI: C4025703
Disease: Calcification of the small brain vessels
Calcification of the small brain vessels 		3 0 3 0.19 0 0
CUI: C0750951
Disease: Lenticulostriate Disorders
Lenticulostriate Disorders 		12 0 4 0.17 0 0
CUI: C4551624
Disease: Idiopathic basal ganglia calcification 1
Idiopathic basal ganglia calcification 1 		6 0 3 0.16 0 0
CUI: C1969913
Disease: Generalized hyperkeratosis
Generalized hyperkeratosis 		16 0 4 0.14 0 0
CUI: C0015371
Disease: Extrapyramidal Disorders
Extrapyramidal Disorders 		27 0 5 0.13 0 0
CUI: C0851409
Disease: Glaucoma and ocular hypertension
Glaucoma and ocular hypertension 		10 0 3 0.13 0 0
CUI: C0004782
Disease: Basal Ganglia Diseases
Basal Ganglia Diseases 		19 0 4 0.13 0 0
CUI: C0432315
Disease: Epidermolysis bullosa simplex herpetiformis
Epidermolysis bullosa simplex herpetiformis 		2 0 2 0.12 0 0
CUI: C3715082
Disease: EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 1
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 1 		2 0 2 0.12 0 0
CUI: C3809084
Disease: MYOFIBROMATOSIS, INFANTILE, 2
MYOFIBROMATOSIS, INFANTILE, 2 		2 0 2 0.12 0 0
CUI: C4302031
Disease: Basal epidermolysis bullosa simplex
Basal epidermolysis bullosa simplex 		2 0 2 0.12 0 0
CUI: C0040046
Disease: Thrombophlebitis
Thrombophlebitis 		3 0 2 0.12 0 0
CUI: C1389280
Disease: Basal ganglia calcification
Basal ganglia calcification 		22 0 4 0.12 0 0
CUI: C0002982
Disease: Angioid Streaks
Angioid Streaks 		13 0 3 0.12 0 0
CUI: C0751304
Disease: Parasagittal Meningioma
Parasagittal Meningioma 		13 0 3 0.12 0 0
CUI: C0006281
Disease: Congenital bronchogenic cyst
Congenital bronchogenic cyst 		4 0 2 0.11 0 0
CUI: C0079295
Disease: Epidermolysis Bullosa Herpetiformis Dowling-Meara
Epidermolysis Bullosa Herpetiformis Dowling-Meara 		4 0 2 0.11 0 0
CUI: C0080333
Disease: Weber-Cockayne Syndrome
Weber-Cockayne Syndrome 		4 0 2 0.11 0 0
CUI: C0240341
Disease: Micrographia
Micrographia 		14 0 3 0.11 0 0
CUI: C1403996
Disease: Squamous cell metaplasia
Squamous cell metaplasia 		4 0 2 0.11 0 0
CUI: C1832926
Disease: EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE (disorder)
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE (disorder) 		4 0 2 0.11 0 0
CUI: C1863411
Disease: Retinal hamartoma
Retinal hamartoma 		4 0 2 0.11 0 0