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: C0221025
Disease: Kasabach-Merritt syndrome
Kasabach-Merritt syndrome 		6 0 4 0.31 0 0
CUI: C0687140
Disease: Hemangioma of skin
Hemangioma of skin 		8 0 3 0.19 0 0
CUI: C1856892
Disease: Facial Dysmorphism with Multiple Malformations
Facial Dysmorphism with Multiple Malformations 		2 0 2 0.18 0 0
CUI: C1707400
Disease: Classic medulloblastoma
Classic medulloblastoma 		3 0 2 0.17 0 0
CUI: C4329301
Disease: Anastomosing Hemangioma
Anastomosing Hemangioma 		3 0 2 0.17 0 0
CUI: C0685682
Disease: Single naris
Single naris 		5 0 2 0.14 0 0
CUI: C0238015
Disease: Autonomic Dysreflexia
Autonomic Dysreflexia 		7 0 2 0.12 0 0
CUI: C0265633
Disease: Congenital absence of tibia
Congenital absence of tibia 		7 0 2 0.12 0 0
CUI: C0343082
Disease: Senile angioma
Senile angioma 		8 0 2 0.12 0 0
CUI: C1861443
Disease: Facial hemangioma
Facial hemangioma 		9 0 2 0.11 0 0
CUI: C0263218
Disease: Pyogenic granuloma of skin
Pyogenic granuloma of skin 		10 0 2 0.11 0 0
CUI: C0265191
Disease: Chronic acquired lymphedema
Chronic acquired lymphedema 		12 0 2 9.5E-02 0 0
CUI: C0948249
Disease: Femoral artery occlusion
Femoral artery occlusion 		12 0 2 9.5E-02 0 0
CUI: C0085653
Disease: Pyogenic granuloma
Pyogenic granuloma 		13 4 2 9.1E-02 1 0.25
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 0 1 9.1E-02 0 0
CUI: C0265974
Disease: Birthmark
Birthmark 		1 0 1 9.1E-02 0 0
CUI: C0266094
Disease: Congenital macrocheilia
Congenital macrocheilia 		1 0 1 9.1E-02 0 0
CUI: C0267024
Disease: Hypertrophy of lip
Hypertrophy of lip 		1 0 1 9.1E-02 0 0
CUI: C0332972
Disease: Congenital vascular proliferation
Congenital vascular proliferation 		1 0 1 9.1E-02 0 0
CUI: C0341154
Disease: Esophageal atresia with tracheoesophageal fistula (disorder)
Esophageal atresia with tracheoesophageal fistula (disorder) 		1 0 1 9.1E-02 0 0
CUI: C0346073
Disease: Tufted angioma of skin
Tufted angioma of skin 		1 0 1 9.1E-02 0 0
CUI: C0349623
Disease: Primary Melanocytic Lesion of Meninges
Primary Melanocytic Lesion of Meninges 		1 0 1 9.1E-02 0 0
CUI: C0522035
Disease: Edema of the upper extremity
Edema of the upper extremity 		1 0 1 9.1E-02 0 0
CUI: C0852973
Disease: Ventricular hypoplasia
Ventricular hypoplasia 		1 0 1 9.1E-02 0 0
CUI: C1370832
Disease: Recurrent Childhood Hepatocellular Carcinoma
Recurrent Childhood Hepatocellular Carcinoma 		1 0 1 9.1E-02 0 0