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: C0549608
Disease: VEINS/LYMPHATICS
VEINS/LYMPHATICS 		1 0 1 0.11 0 0
CUI: C0861199
Disease: Lymphoplasmacytoid immunocytoma
Lymphoplasmacytoid immunocytoma 		1 0 1 0.11 0 0
CUI: C0861999
Disease: Centrocytic (mantle cell) lymphoma (Kiel classification)
Centrocytic (mantle cell) lymphoma (Kiel classification) 		1 0 1 0.11 0 0
CUI: C1266046
Disease: Atypical follicular adenoma
Atypical follicular adenoma 		1 0 1 0.11 0 0
CUI: C1306574
Disease: Botryoid rhabdomyosarcoma
Botryoid rhabdomyosarcoma 		1 0 1 0.11 0 0
CUI: C1333081
Disease: Colloid Carcinoma of the Pancreas
Colloid Carcinoma of the Pancreas 		1 0 1 0.11 0 0
CUI: C1333308
Disease: Distal Bile Duct Carcinoma
Distal Bile Duct Carcinoma 		1 0 1 0.11 0 0
CUI: C1333786
Disease: Gastric Precancerous Condition
Gastric Precancerous Condition 		1 0 1 0.11 0 0
CUI: C1333940
Disease: Head and Neck Basaloid Carcinoma
Head and Neck Basaloid Carcinoma 		1 0 1 0.11 0 0
CUI: C1334413
Disease: Low Grade Ductal Breast Carcinoma In Situ
Low Grade Ductal Breast Carcinoma In Situ 		1 0 1 0.11 0 0
CUI: C1515107
Disease: Synchronous Bilateral Breast Carcinoma
Synchronous Bilateral Breast Carcinoma 		1 0 1 0.11 0 0
CUI: C1704453
Disease: Oncocytic Schneiderian papilloma
Oncocytic Schneiderian papilloma 		1 0 1 0.11 0 0
CUI: C1838329
Disease: APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS
APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS 		1 0 1 0.11 0 0
CUI: C1842881
Disease: Dilated aortic root
Dilated aortic root 		1 0 1 0.11 0 0
CUI: C1853398
Disease: Spasticity of pharyngeal muscles
Spasticity of pharyngeal muscles 		1 0 1 0.11 0 0
CUI: C1853404
Disease: Spasticity of facial muscles
Spasticity of facial muscles 		1 0 1 0.11 0 0
CUI: C1865864
Disease: AMYOTROPHIC LATERAL SCLEROSIS 5
AMYOTROPHIC LATERAL SCLEROSIS 5 		1 0 1 0.11 0 0
CUI: C2721606
Disease: Bladder dysplasia
Bladder dysplasia 		1 0 1 0.11 0 0
CUI: C2749936
Disease: SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE (disorder) 		1 0 1 0.11 0 0
CUI: C2750729
Disease: Amyotrophic Lateral Sclerosis 6, Autosomal Recessive
Amyotrophic Lateral Sclerosis 6, Autosomal Recessive 		1 0 1 0.11 0 0
CUI: C2931786
Disease: Amyotrophic lateral sclerosis, type 6
Amyotrophic lateral sclerosis, type 6 		1 0 1 0.11 0 0
CUI: C2931821
Disease: Nakamura Osame syndrome
Nakamura Osame syndrome 		1 0 1 0.11 0 0
CUI: C3280587
Disease: AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE
AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE 		1 0 1 0.11 0 0
CUI: C3539195
Disease: TREMOR, HEREDITARY ESSENTIAL, 4
TREMOR, HEREDITARY ESSENTIAL, 4 		1 0 1 0.11 0 0
CUI: C3658353
Disease: Nodding Syndrome
Nodding Syndrome 		1 0 1 0.11 0 0