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: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 5.9E-02 0 0
CUI: C0024900
Disease: Mastocytosis, Bullous
Mastocytosis, Bullous 		1 0 1 5.9E-02 0 0
CUI: C0031557
Disease: Phlegmon
Phlegmon 		1 0 1 5.9E-02 0 0
CUI: C0155526
Disease: Cochlear otosclerosis
Cochlear otosclerosis 		1 0 1 5.9E-02 0 0
CUI: C0178650
Disease: Gammopathy
Gammopathy 		1 0 1 5.9E-02 0 0
CUI: C0206672
Disease: Hidrocystoma
Hidrocystoma 		1 0 1 5.9E-02 0 0
CUI: C0240583
Disease: Short upturned nose
Short upturned nose 		1 0 1 5.9E-02 0 0
CUI: C0263402
Disease: Telangiectasia macularis eruptiva perstans
Telangiectasia macularis eruptiva perstans 		1 0 1 5.9E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 5.9E-02 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome 		1 0 1 5.9E-02 0 0
CUI: C0265974
Disease: Birthmark
Birthmark 		1 0 1 5.9E-02 0 0
CUI: C0266004
Disease: Knuckle pads, leuconychia and sensorineural deafness
Knuckle pads, leuconychia and sensorineural deafness 		1 21 1 5.9E-02 1 3.3E-02
CUI: C0266094
Disease: Congenital macrocheilia
Congenital macrocheilia 		1 0 1 5.9E-02 0 0
CUI: C0267024
Disease: Hypertrophy of lip
Hypertrophy of lip 		1 0 1 5.9E-02 0 0
CUI: C0276270
Disease: Oral papillomatosis
Oral papillomatosis 		1 0 1 5.9E-02 0 0
CUI: C0280301
Disease: Hard Palate Squamous Cell Carcinoma
Hard Palate Squamous Cell Carcinoma 		1 0 1 5.9E-02 0 0
CUI: C0332972
Disease: Congenital vascular proliferation
Congenital vascular proliferation 		1 0 1 5.9E-02 0 0
CUI: C0334432
Disease: Nonpigmented nevus
Nonpigmented nevus 		1 0 1 5.9E-02 0 0
CUI: C0341215
Disease: Gastroduodenal intussusception
Gastroduodenal intussusception 		1 0 1 5.9E-02 0 0
CUI: C0343115
Disease: Skin Mastocytoma
Skin Mastocytoma 		1 0 1 5.9E-02 0 0
CUI: C0349623
Disease: Primary Melanocytic Lesion of Meninges
Primary Melanocytic Lesion of Meninges 		1 0 1 5.9E-02 0 0
CUI: C0391816
Disease: Tietz syndrome
Tietz syndrome 		1 5 1 5.9E-02 1 7.1E-02
CUI: C0395976
Disease: Hearing loss associated with syndrome
Hearing loss associated with syndrome 		1 0 1 5.9E-02 0 0
CUI: C0406821
Disease: Rhabdomyomatous mesenchymal hamartoma
Rhabdomyomatous mesenchymal hamartoma 		1 0 1 5.9E-02 0 0
CUI: C0413235
Disease: Idiopathic anaphylaxis
Idiopathic anaphylaxis 		1 0 1 5.9E-02 0 0