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: C0149640
Disease: Cecum Carcinoma
Cecum Carcinoma 		1 0 1 5.0E-02 0 0
CUI: C0149881
Disease: Epididymo-orchitis
Epididymo-orchitis 		1 0 1 5.0E-02 0 0
CUI: C0221218
Disease: Fordyce's disease
Fordyce's disease 		1 0 1 5.0E-02 0 0
CUI: C0268486
Disease: Hereditary hypertyrosinemia
Hereditary hypertyrosinemia 		1 0 1 5.0E-02 0 0
CUI: C0700509
Disease: Chronic peptic ulcer
Chronic peptic ulcer 		1 0 1 5.0E-02 0 0
CUI: C1263777
Disease: Neoplasm of body of uterus
Neoplasm of body of uterus 		1 0 1 5.0E-02 0 0
CUI: C1519702
Disease: Turcot Syndrome Type 1
Turcot Syndrome Type 1 		1 0 1 5.0E-02 0 0
CUI: C1711192
Disease: Sporadic Gastric Adenocarcinoma
Sporadic Gastric Adenocarcinoma 		1 0 1 5.0E-02 0 0
CUI: C1837464
Disease: Small eyes
Small eyes 		1 0 1 5.0E-02 0 0
CUI: C1848695
Disease: Episodic peripheral neuropathy
Episodic peripheral neuropathy 		1 0 1 5.0E-02 0 0
CUI: C1849198
Disease: Opacification of the corneal epithelium
Opacification of the corneal epithelium 		1 0 1 5.0E-02 0 0
CUI: C1856796
Disease: Estren-Dameshek Variant of Fanconi Anemia
Estren-Dameshek Variant of Fanconi Anemia 		1 0 1 5.0E-02 0 0
CUI: C1856797
Disease: Estren-Dameshek Variant of Fanconi Pancytopenia
Estren-Dameshek Variant of Fanconi Pancytopenia 		1 0 1 5.0E-02 0 0
CUI: C2033037
Disease: Pancreatic Vipoma
Pancreatic Vipoma 		1 0 1 5.0E-02 0 0
CUI: C3272608
Disease: Colorectal Large Cell Neuroendocrine Carcinoma
Colorectal Large Cell Neuroendocrine Carcinoma 		1 0 1 5.0E-02 0 0
CUI: C3280598
Disease: SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY 		1 0 1 5.0E-02 0 0
CUI: C3280612
Disease: NEPHRONOPHTHISIS 13
NEPHRONOPHTHISIS 13 		1 0 1 5.0E-02 0 0
CUI: C3554576
Disease: FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE
FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE 		1 0 1 5.0E-02 0 0
CUI: C3715192
Disease: ANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME
ANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME 		1 0 1 5.0E-02 0 0
CUI: C3899669
Disease: Childhood Colorectal Carcinoma
Childhood Colorectal Carcinoma 		1 0 1 5.0E-02 0 0
CUI: C4225376
Disease: SENIOR-LOKEN SYNDROME 8
SENIOR-LOKEN SYNDROME 8 		1 0 1 5.0E-02 0 0
CUI: C4725945
Disease: Mutation-Negative Lynch Syndrome
Mutation-Negative Lynch Syndrome 		1 0 1 5.0E-02 0 0
CUI: C4755276
Disease: Primary CD59 deficiency
Primary CD59 deficiency 		1 0 1 5.0E-02 0 0
CUI: C0271333
Disease: Orbital lymphoma
Orbital lymphoma 		2 0 1 4.8E-02 0 0
CUI: C0278798
Disease: Endometrial neoplasm malignant stage I
Endometrial neoplasm malignant stage I 		2 0 1 4.8E-02 0 0