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: C0001145
Disease: Acne Keloid
Acne Keloid 		1 0 1 1.3E-02 0 0
CUI: C0010334
Disease: Crisscross Heart
Crisscross Heart 		1 0 1 1.3E-02 0 0
CUI: C0031557
Disease: Phlegmon
Phlegmon 		1 0 1 1.3E-02 0 0
CUI: C0031925
Disease: Pilonidal Cyst
Pilonidal Cyst 		1 0 1 1.3E-02 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 1.3E-02 0 0
CUI: C0043379
Disease: XYY Karyotype
XYY Karyotype 		1 0 1 1.3E-02 0 0
CUI: C0155526
Disease: Cochlear otosclerosis
Cochlear otosclerosis 		1 0 1 1.3E-02 0 0
CUI: C0155563
Disease: Rheumatic mitral regurgitation
Rheumatic mitral regurgitation 		1 0 1 1.3E-02 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur 		1 0 1 1.3E-02 0 0
CUI: C0241424
Disease: Tongue biting
Tongue biting 		1 0 1 1.3E-02 0 0
CUI: C0241633
Disease: Vaginal dryness
Vaginal dryness 		1 0 1 1.3E-02 0 0
CUI: C0263583
Disease: Idiopathic guttate hypomelanosis
Idiopathic guttate hypomelanosis 		1 0 1 1.3E-02 0 0
CUI: C0263925
Disease: Iliac crest spur
Iliac crest spur 		1 0 1 1.3E-02 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta 		1 0 1 1.3E-02 0 0
CUI: C0266004
Disease: Knuckle pads, leuconychia and sensorineural deafness
Knuckle pads, leuconychia and sensorineural deafness 		1 0 1 1.3E-02 0 0
CUI: C0268371
Disease: Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails 		1 0 1 1.3E-02 0 0
CUI: C0268375
Disease: Autosomal dominant epidermolysis bullosa simplex
Autosomal dominant epidermolysis bullosa simplex 		1 0 1 1.3E-02 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula 		1 0 1 1.3E-02 0 0
CUI: C0270804
Disease: Spastic Diplegia Cerebral Palsy
Spastic Diplegia Cerebral Palsy 		1 0 1 1.3E-02 0 0
CUI: C0280301
Disease: Hard Palate Squamous Cell Carcinoma
Hard Palate Squamous Cell Carcinoma 		1 0 1 1.3E-02 0 0
CUI: C0332778
Disease: Diastasis, Bone
Diastasis, Bone 		1 0 1 1.3E-02 0 0
CUI: C0340031
Disease: Mucociliary clearance defect
Mucociliary clearance defect 		1 0 1 1.3E-02 0 0
CUI: C0342278
Disease: Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans
Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 		1 0 1 1.3E-02 0 0
CUI: C0343111
Disease: Naegeli syndrome
Naegeli syndrome 		1 0 1 1.3E-02 0 0
CUI: C0349477
Disease: Transient neonatal hypothyroidism
Transient neonatal hypothyroidism 		1 0 1 1.3E-02 0 0