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: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 0 1 0.33 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 1 1 0.33 1 0.50
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle 		1 0 1 0.33 0 0
CUI: C0259782
Disease: Telangiectatic osteosarcoma
Telangiectatic osteosarcoma 		1 0 1 0.33 0 0
CUI: C0432149
Disease: Lumbar hemivertebra
Lumbar hemivertebra 		1 0 1 0.33 0 0
CUI: C0495640
Disease: Congenital malformation syndromes involving early overgrowth
Congenital malformation syndromes involving early overgrowth 		1 0 1 0.33 0 0
CUI: C1274594
Disease: Lichenoid actinic keratosis
Lichenoid actinic keratosis 		1 0 1 0.33 0 0
CUI: C1333286
Disease: Diencephalic Neoplasm
Diencephalic Neoplasm 		1 0 1 0.33 0 0
CUI: C1334664
Disease: Mediastinal Lymphangioma
Mediastinal Lymphangioma 		1 0 1 0.33 0 0
CUI: C1335389
Disease: Lipomatosis of Nerve
Lipomatosis of Nerve 		1 0 1 0.33 0 0
CUI: C1845146
Disease: Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate 		1 0 1 0.33 0 0
CUI: C2751313
Disease: CLAPO Syndrome
CLAPO Syndrome 		1 5 1 0.33 1 0.17
CUI: C2752042
Disease: Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi
Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 		1 5 1 0.33 1 0.17
CUI: C3550024
Disease: MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME, SOMATIC
MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME, SOMATIC 		1 0 1 0.33 0 0
CUI: C3554518
Disease: COWDEN SYNDROME 5
COWDEN SYNDROME 5 		1 0 1 0.33 0 0
CUI: C3838879
Disease: Tubulolobular carcinoma
Tubulolobular carcinoma 		1 0 1 0.33 0 0
CUI: C3843745
Disease: Squamous cell (epidermoid) carcinoma
Squamous cell (epidermoid) carcinoma 		1 0 1 0.33 0 0
CUI: C4016104
Disease: HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA 		1 0 1 0.33 0 0
CUI: C4520854
Disease: Stage I Colorectal Cancer AJCC v6 and v7
Stage I Colorectal Cancer AJCC v6 and v7 		1 0 1 0.33 0 0
CUI: C4749056
Disease: MACRODACTYLY, SOMATIC
MACRODACTYLY, SOMATIC 		1 1 1 0.33 1 0.50
CUI: C0011645
Disease: Dermatosis Papulosa Nigra
Dermatosis Papulosa Nigra 		2 0 1 0.25 0 0
CUI: C0241665
Disease: Abnormal venous morphology
Abnormal venous morphology 		2 0 1 0.25 0 0
CUI: C0266166
Disease: Congenital duplication of intestine
Congenital duplication of intestine 		2 0 1 0.25 0 0
CUI: C0302894
Disease: Stucco keratosis
Stucco keratosis 		2 0 1 0.25 0 0
CUI: C0334067
Disease: Non-Ossifying Fibroma
Non-Ossifying Fibroma 		2 0 1 0.25 0 0