Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Dense calcifications in the cerebellar dentate nucleus
3 0 3 1.00 0 0
Idiopathic basal ganglia calcification 1
6 0 3 0.50 0 0
CUI: C0042907
Disease: Vitreous Detachment
Vitreous Detachment
1 0 1 0.33 0 0
CUI: C0262477
Disease: Eye problem
Eye problem
1 0 1 0.33 0 0
CUI: C0278714
Disease: stage IV Wilms tumor
stage IV Wilms tumor
1 0 1 0.33 0 0
Dermatofibrosarcoma Protuberans, Myxoid
1 0 1 0.33 0 0
CUI: C0521668
Disease: Primary Thunderclap Headache
Primary Thunderclap Headache
1 0 1 0.33 0 0
CUI: C0685661
Disease: Congenital anomaly of ischium
Congenital anomaly of ischium
1 0 1 0.33 0 0
CUI: C0856900
Disease: Sarcoma of skin
Sarcoma of skin
1 0 1 0.33 0 0
CUI: C1856231
Disease: Thin calvarium
Thin calvarium
1 0 1 0.33 0 0
CUI: C1866182
Disease: Penttinen-Aula syndrome
Penttinen-Aula syndrome
1 0 1 0.33 0 0
Myeloid neoplasm with beta-type platelet-derived growth factor receptor gene rearrangement
1 0 1 0.33 0 0
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4
1 0 1 0.33 0 0
Pdgfrb-Associated Chronic Eosinophilic Leukemia
1 0 1 0.33 0 0
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5
1 0 1 0.33 0 0
CUI: C3840151
Disease: Congenital glenoid dysplasia
Congenital glenoid dysplasia
1 0 1 0.33 0 0
CUI: C4551572
Disease: MYOFIBROMATOSIS, INFANTILE, 1
MYOFIBROMATOSIS, INFANTILE, 1
1 0 1 0.33 0 0
CUI: C0393590
Disease: Fahr's syndrome (disorder)
Fahr's syndrome (disorder)
10 0 3 0.30 0 0
CUI: C0017566
Disease: Gingival Hyperplasia
Gingival Hyperplasia
2 0 1 0.25 0 0
CUI: C0334139
Disease: Microglial nodules
Microglial nodules
2 0 1 0.25 0 0
Pigmented Dermatofibrosarcoma Protuberans (Bednar Tumor)
2 0 1 0.25 0 0
CUI: C0522205
Disease: Sexual inhibition
Sexual inhibition
2 0 1 0.25 0 0
CUI: C0750951
Disease: Lenticulostriate Disorders
Lenticulostriate Disorders
12 0 3 0.25 0 0
Conventional Dermatofibrosarcoma Protuberans
2 0 1 0.25 0 0
Soft tissue swelling of interphalangeal joints
2 0 1 0.25 0 0