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: C0025060
Disease: Mediastinal Cyst
Mediastinal Cyst
1 0 1 0.17 0 0
CUI: C0238525
Disease: Sarcoma of vulva
Sarcoma of vulva
1 0 1 0.17 0 0
CUI: C0268248
Disease: Niemann-Pick Disease, Type E
Niemann-Pick Disease, Type E
1 0 1 0.17 0 0
Dermatofibrosarcoma Protuberans, Myxoid
1 0 1 0.17 0 0
CUI: C0349582
Disease: Trigeminal schwannoma
Trigeminal schwannoma
1 0 1 0.17 0 0
CUI: C0476337
Disease: Blood gases abnormal
Blood gases abnormal
1 0 1 0.17 0 0
CUI: C0855040
Disease: Epithelioid sarcoma non-metastatic
Epithelioid sarcoma non-metastatic
1 0 1 0.17 0 0
CUI: C0856900
Disease: Sarcoma of skin
Sarcoma of skin
1 0 1 0.17 0 0
CUI: C1136041
Disease: Familial Acoustic Neuroma
Familial Acoustic Neuroma
1 0 1 0.17 0 0
CUI: C1136043
Disease: Schwannoma, Acoustic, Bilateral
Schwannoma, Acoustic, Bilateral
1 0 1 0.17 0 0
CUI: C1333306
Disease: Distal-Type Epithelioid Sarcoma
Distal-Type Epithelioid Sarcoma
1 0 1 0.17 0 0
CUI: C1709579
Disease: Pleural Synovial Sarcoma
Pleural Synovial Sarcoma
1 0 1 0.17 0 0
CUI: C1836326
Disease: Teratoid Tumor, Atypical
Teratoid Tumor, Atypical
1 0 1 0.17 0 0
RHABDOID TUMOR PREDISPOSITION SYNDROME 1 (disorder)
1 0 1 0.17 0 0
Diffuse reticular or finely nodular infiltrations
1 0 1 0.17 0 0
Juvenile posterior subcapsular lenticular opacities
1 0 1 0.17 0 0
CUI: C1863653
Disease: Unilateral vestibular Schwannoma
Unilateral vestibular Schwannoma
1 0 1 0.17 0 0
NIEMANN-PICK DISEASE, INTERMEDIATE, PROTRACTED NEUROVISCERAL (disorder)
1 0 1 0.17 0 0
CUI: C2721740
Disease: Ventilation perfusion mismatch
Ventilation perfusion mismatch
1 0 1 0.17 0 0
CUI: C2750405
Disease: Malignant Rhabdoid Tumor, Somatic
Malignant Rhabdoid Tumor, Somatic
1 0 1 0.17 0 0
CUI: C3272425
Disease: Gastric Schwannoma
Gastric Schwannoma
1 0 1 0.17 0 0
MENTAL RETARDATION, AUTOSOMAL DOMINANT 15
1 0 1 0.17 0 0
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5
1 0 1 0.17 0 0
CUI: C3810474
Disease: Occasional neurofibromas
Occasional neurofibromas
1 0 1 0.17 0 0
CUI: C3840151
Disease: Congenital glenoid dysplasia
Congenital glenoid dysplasia
1 0 1 0.17 0 0