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: C0235267
Disease: Redness of eye
Redness of eye 		1 0 1 1.0E-01 0 0
CUI: C0238518
Disease: Squamous cell carcinoma of vagina
Squamous cell carcinoma of vagina 		1 0 1 1.0E-01 0 0
CUI: C0263583
Disease: Idiopathic guttate hypomelanosis
Idiopathic guttate hypomelanosis 		1 0 1 1.0E-01 0 0
CUI: C0347493
Disease: Cervix adenomatous polyp
Cervix adenomatous polyp 		1 0 1 1.0E-01 0 0
CUI: C0495106
Disease: Vulval intraepithelial neoplasia grade 1
Vulval intraepithelial neoplasia grade 1 		1 0 1 1.0E-01 0 0
CUI: C0520474
Disease: Aseptic Necrosis of Bone
Aseptic Necrosis of Bone 		1 0 1 1.0E-01 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 1.0E-01 0 0
CUI: C0741900
Disease: carcinoma sarcoma
carcinoma sarcoma 		1 0 1 1.0E-01 0 0
CUI: C0948075
Disease: Anal infection
Anal infection 		1 0 1 1.0E-01 0 0
CUI: C1168331
Disease: Apical myocardial infarction
Apical myocardial infarction 		1 0 1 1.0E-01 0 0
CUI: C1332887
Disease: Central Nervous System Melanocytic Neoplasm
Central Nervous System Melanocytic Neoplasm 		1 0 1 1.0E-01 0 0
CUI: C1336109
Disease: Stage IA1 Cervical Cancer
Stage IA1 Cervical Cancer 		1 0 1 1.0E-01 0 0
CUI: C1510961
Disease: Atypical neurofibroma
Atypical neurofibroma 		1 0 1 1.0E-01 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 1.0E-01 0 0
CUI: C1835042
Disease: Melanoma astrocytoma syndrome
Melanoma astrocytoma syndrome 		1 0 1 1.0E-01 0 0
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		1 0 1 1.0E-01 0 0
CUI: C1835253
Disease: Hyperkeratosis over edematous areas
Hyperkeratosis over edematous areas 		1 0 1 1.0E-01 0 0
CUI: C1837206
Disease: Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly
Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly 		1 0 1 1.0E-01 0 0
CUI: C1838547
Disease: MELANOMA-PANCREATIC CANCER SYNDROME
MELANOMA-PANCREATIC CANCER SYNDROME 		1 0 1 1.0E-01 0 0
CUI: C1847507
Disease: Paroxysmal lethargy
Paroxysmal lethargy 		1 0 1 1.0E-01 0 0
CUI: C1850158
Disease: Interphalangeal joint erosions
Interphalangeal joint erosions 		1 0 1 1.0E-01 0 0
CUI: C1850159
Disease: Widened metacarpal shaft
Widened metacarpal shaft 		1 0 1 1.0E-01 0 0
CUI: C1850162
Disease: Thin metatarsal cortices
Thin metatarsal cortices 		1 0 1 1.0E-01 0 0
CUI: C3149117
Disease: GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE
GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE 		1 0 1 1.0E-01 0 0
CUI: C3532172
Disease: Fetal heart failure
Fetal heart failure 		1 0 1 1.0E-01 0 0