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: C1096654
Disease: Cardiac fibroma
Cardiac fibroma 		4 0 2 0.18 0 0
CUI: C0271633
Disease: Disorder of endocrine pancreas
Disorder of endocrine pancreas 		6 0 2 0.15 0 0
CUI: C0424304
Disease: Inappropriate laughter
Inappropriate laughter 		7 2 2 0.14 1 0.17
CUI: C3665983
Disease: Oral aversion
Oral aversion 		7 4 2 0.14 2 0.29
CUI: C4022873
Disease: Small pituitary gland
Small pituitary gland 		7 4 2 0.14 1 0.12
CUI: C4022919
Disease: Appendicular hypotonia
Appendicular hypotonia 		8 8 2 0.13 1 8.3E-02
CUI: C0271292
Disease: Corneal hypoesthesia
Corneal hypoesthesia 		1 0 1 0.11 0 0
CUI: C0279697
Disease: salivary gland squamous cell carcinoma
salivary gland squamous cell carcinoma 		1 0 1 0.11 0 0
CUI: C0334338
Disease: Endometrioid adenoma, borderline malignancy
Endometrioid adenoma, borderline malignancy 		1 0 1 0.11 0 0
CUI: C0334566
Disease: Ghost Cell Odontogenic Carcinoma
Ghost Cell Odontogenic Carcinoma 		1 0 1 0.11 0 0
CUI: C0405124
Disease: Nuchal Cord
Nuchal Cord 		1 1 1 0.11 1 0.20
CUI: C0406571
Disease: Superficial fibromatosis
Superficial fibromatosis 		1 0 1 0.11 0 0
CUI: C0877306
Disease: Iris hyperpigmentation
Iris hyperpigmentation 		1 0 1 0.11 0 0
CUI: C1275420
Disease: Extra-abdominal fibromatosis
Extra-abdominal fibromatosis 		1 0 1 0.11 0 0
CUI: C1333117
Disease: Colorectal Tubular Adenoma
Colorectal Tubular Adenoma 		1 0 1 0.11 0 0
CUI: C1334963
Disease: Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma
Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma 		1 0 1 0.11 0 0
CUI: C1368295
Disease: Malignant basal cell tumor
Malignant basal cell tumor 		1 0 1 0.11 0 0
CUI: C1691013
Disease: Macular corneal dystrophy Type II (disorder)
Macular corneal dystrophy Type II (disorder) 		1 0 1 0.11 0 0
CUI: C1704219
Disease: Dentinogenic Ghost Cell Tumor
Dentinogenic Ghost Cell Tumor 		1 0 1 0.11 0 0
CUI: C1834038
Disease: Schilbach-Rott Syndrome
Schilbach-Rott Syndrome 		1 0 1 0.11 0 0
CUI: C1834930
Disease: Fusion of the left and right thalami
Fusion of the left and right thalami 		1 0 1 0.11 0 0
CUI: C1835820
Disease: HOLOPROSENCEPHALY 7
HOLOPROSENCEPHALY 7 		1 0 1 0.11 0 0
CUI: C1847886
Disease: Anomalous branches of internal carotid artery
Anomalous branches of internal carotid artery 		1 1 1 0.11 1 0.20
CUI: C1851085
Disease: Severe expressive language delay
Severe expressive language delay 		11 7 2 0.11 2 0.20
CUI: C1854934
Disease: Progressive alveolar ridge hypertropy
Progressive alveolar ridge hypertropy 		1 0 1 0.11 0 0