Source: BEFREE ×
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: C1961121
Disease: Congenital vascular anomaly
Congenital vascular anomaly 		42 0 21 0.32 0 0
CUI: C0265950
Disease: Venous malformation
Venous malformation 		35 3 13 0.19 1 0.14
CUI: C2937220
Disease: Congenital abnormality of vein
Congenital abnormality of vein 		35 3 13 0.19 1 0.14
CUI: C0038505
Disease: Sturge-Weber Syndrome
Sturge-Weber Syndrome 		25 0 11 0.19 0 0
CUI: C0265316
Disease: Neurocutaneous Syndromes
Neurocutaneous Syndromes 		26 0 11 0.18 0 0
CUI: C0039445
Disease: Hereditary hemorrhagic telangiectasia
Hereditary hemorrhagic telangiectasia 		42 0 13 0.18 0 0
CUI: C0272139
Disease: Erythrocytosis due to low atmospheric pressure
Erythrocytosis due to low atmospheric pressure 		25 0 10 0.17 0 0
CUI: C0003857
Disease: Congenital arteriovenous malformation
Congenital arteriovenous malformation 		127 23 23 0.15 2 7.7E-02
CUI: C0235752
Disease: Port-Wine Stain
Port-Wine Stain 		9 0 7 0.15 0 0
CUI: C4728213
Disease: PIK3CA related overgrowth spectrum
PIK3CA related overgrowth spectrum 		11 0 7 0.14 0 0
CUI: C0398368
Disease: Lymphatic Abnormalities
Lymphatic Abnormalities 		29 0 9 0.14 0 0
CUI: C0024221
Disease: Lymphangioma
Lymphangioma 		13 0 7 0.14 0 0
CUI: C1846385
Disease: FOCAL CORTICAL DYSPLASIA OF TAYLOR
FOCAL CORTICAL DYSPLASIA OF TAYLOR 		13 0 7 0.14 0 0
CUI: C0238348
Disease: Squamous cell carcinoma of penis
Squamous cell carcinoma of penis 		40 0 10 0.13 0 0
CUI: C0267370
Disease: Angiodysplasia of colon
Angiodysplasia of colon 		6 0 6 0.13 0 0
CUI: C1959582
Disease: PTEN Hamartoma Tumor Syndrome
PTEN Hamartoma Tumor Syndrome 		15 0 7 0.13 0 0
CUI: C0085411
Disease: Angiodysplasia
Angiodysplasia 		7 0 6 0.13 0 0
CUI: C4285730
Disease: Activated PI3 kinase delta syndrome
Activated PI3 kinase delta syndrome 		7 0 6 0.13 0 0
CUI: C4551861
Disease: Telangiectasia, Hereditary Hemorrhagic, Type 1
Telangiectasia, Hereditary Hemorrhagic, Type 1 		7 0 6 0.13 0 0
CUI: C1865285
Disease: Megalencephaly cutis marmorata telangiectatica congenita
Megalencephaly cutis marmorata telangiectatica congenita 		16 0 7 0.13 0 0
CUI: C3897752
Disease: Recurrent Childhood Glioblastoma
Recurrent Childhood Glioblastoma 		51 0 11 0.13 0 0
CUI: C4288305
Disease: Recurrent Glioblastoma
Recurrent Glioblastoma 		51 0 11 0.13 0 0
CUI: C0085261
Disease: Proteus Syndrome
Proteus Syndrome 		17 0 7 0.13 0 0
CUI: C0017662
Disease: Glomerulonephritis, Membranoproliferative
Glomerulonephritis, Membranoproliferative 		35 0 9 0.13 0 0
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		35 0 9 0.13 0 0