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: C0019618
Disease: Histiocytosis
Histiocytosis 		32 3 20 0.61 2 0.67
CUI: C0019624
Disease: Histiocytosis, Non-Langerhans-Cell
Histiocytosis, Non-Langerhans-Cell 		9 2 5 0.20 2 1.00
CUI: C1531553
Disease: Dendritic cell neoplasm
Dendritic cell neoplasm 		6 2 4 0.17 2 1.00
CUI: C0878675
Disease: Erdheim-Chester Disease
Erdheim-Chester Disease 		29 2 7 0.16 2 1.00
CUI: C3267126
Disease: Trichodysplasia spinulosa
Trichodysplasia spinulosa 		9 0 4 0.15 0 0
CUI: C0263218
Disease: Pyogenic granuloma of skin
Pyogenic granuloma of skin 		10 3 4 0.15 2 0.67
CUI: C0019625
Disease: Sinus histiocytosis
Sinus histiocytosis 		19 2 5 0.14 2 1.00
CUI: C1860991
Disease: NOONAN SYNDROME 3
NOONAN SYNDROME 3 		11 0 4 0.14 0 0
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome 		28 82 6 0.14 1 1.2E-02
CUI: C0279557
Disease: Adenosquamous cell lung cancer
Adenosquamous cell lung cancer 		12 0 4 0.14 0 0
CUI: C0334230
Disease: Malignant tumor, fusiform cell type
Malignant tumor, fusiform cell type 		4 0 3 0.14 0 0
CUI: C0206739
Disease: Epithelioid and spindle cell nevus
Epithelioid and spindle cell nevus 		21 0 5 0.14 0 0
CUI: C0085653
Disease: Pyogenic granuloma
Pyogenic granuloma 		13 4 4 0.13 2 0.50
CUI: C1511104
Disease: Benign Struma Ovarii
Benign Struma Ovarii 		5 0 3 0.13 0 0
CUI: C1266045
Disease: Metanephric adenoma
Metanephric adenoma 		6 2 3 0.12 2 1.00
CUI: C1533022
Disease: Histiocytic proliferation
Histiocytic proliferation 		7 0 3 0.12 0 0
CUI: C4733333
Disease: familial non-medullary thyroid cancer
familial non-medullary thyroid cancer 		17 0 4 0.12 0 0
CUI: C1455705
Disease: Pulmonary Histiocytosis X
Pulmonary Histiocytosis X 		9 2 3 0.11 2 1.00
CUI: C0334586
Disease: Pleomorphic Xanthoastrocytoma
Pleomorphic Xanthoastrocytoma 		42 8 6 0.11 2 0.25
CUI: C3899645
Disease: Childhood Pleomorphic Xanthoastrocytoma
Childhood Pleomorphic Xanthoastrocytoma 		42 7 6 0.11 2 0.29
CUI: C1849452
Disease: SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder)
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder) 		11 0 3 0.10 0 0
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1 		23 0 4 1.0E-01 0 0
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		47 0 6 9.7E-02 0 0
CUI: C0349633
Disease: Hairy cell leukemia variant
Hairy cell leukemia variant 		13 2 3 9.7E-02 2 1.00
CUI: C1969623
Disease: NEUROFIBROMATOSIS, TYPE 1-LIKE SYNDROME
NEUROFIBROMATOSIS, TYPE 1-LIKE SYNDROME 		13 0 3 9.7E-02 0 0