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: C2748527
Disease: KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (disorder)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (disorder) 		4 0 1 1.0E-01 0 0
CUI: C4330667
Disease: Medulloblastoma, Non-WNT/Non-SHH
Medulloblastoma, Non-WNT/Non-SHH 		4 0 1 1.0E-01 0 0
CUI: C0221409
Disease: Anemia, hereditary spherocytic hemolytic
Anemia, hereditary spherocytic hemolytic 		5 0 1 9.1E-02 0 0
CUI: C0242217
Disease: Calcium Pyrophosphate Dihydrate Deposition
Calcium Pyrophosphate Dihydrate Deposition 		5 0 1 9.1E-02 0 0
CUI: C0340434
Disease: Dystrophic cardiomyopathy
Dystrophic cardiomyopathy 		5 0 1 9.1E-02 0 0
CUI: C0553720
Disease: Spherocytosis
Spherocytosis 		5 0 1 9.1E-02 0 0
CUI: C0856830
Disease: Calcium pyrophosphate arthropathy
Calcium pyrophosphate arthropathy 		5 0 1 9.1E-02 0 0
CUI: C1858593
Disease: Limb-girdle muscular dystrophy, type 2E
Limb-girdle muscular dystrophy, type 2E 		5 0 1 9.1E-02 0 0
CUI: C1998045
Disease: Subclinical hyperthyroidism
Subclinical hyperthyroidism 		5 0 1 9.1E-02 0 0
CUI: C4041147
Disease: Acute exacerbation of chronic obstructive bronchitis
Acute exacerbation of chronic obstructive bronchitis 		5 0 1 9.1E-02 0 0
CUI: C3203509
Disease: Neuropsychiatric syndrome
Neuropsychiatric syndrome 		6 0 1 8.3E-02 0 0
CUI: C3896643
Disease: New Onset Diabetes After Transplant
New Onset Diabetes After Transplant 		6 0 1 8.3E-02 0 0
CUI: C4021526
Disease: Exercise-induced rhabdomyolysis
Exercise-induced rhabdomyolysis 		6 0 1 8.3E-02 0 0
CUI: C0268505
Disease: Ocular albinism, type II
Ocular albinism, type II 		7 0 1 7.7E-02 0 0
CUI: C0271638
Disease: Type 2 diabetes mellitus in obese
Type 2 diabetes mellitus in obese 		7 0 1 7.7E-02 0 0
CUI: C0398568
Disease: Blood group deletion syndrome
Blood group deletion syndrome 		7 0 1 7.7E-02 0 0
CUI: C0751635
Disease: Common Carotid Artery Stenosis
Common Carotid Artery Stenosis 		7 0 1 7.7E-02 0 0
CUI: C1844680
Disease: DEAFNESS-HYPOGONADISM SYNDROME
DEAFNESS-HYPOGONADISM SYNDROME 		7 0 1 7.7E-02 0 0
CUI: C4025184
Disease: Spontaneous hemolytic crises
Spontaneous hemolytic crises 		7 0 1 7.7E-02 0 0
CUI: C4551860
Disease: Ullrich congenital muscular dystrophy
Ullrich congenital muscular dystrophy 		7 0 1 7.7E-02 0 0
CUI: C4554215
Disease: Duchenne or Becker muscular dystrophy
Duchenne or Becker muscular dystrophy 		7 0 1 7.7E-02 0 0
CUI: C1855578
Disease: Exercise-induced muscle cramps
Exercise-induced muscle cramps 		8 0 1 7.1E-02 0 0
CUI: C0153369
Disease: Malignant neoplasm of anterior portion of floor of mouth
Malignant neoplasm of anterior portion of floor of mouth 		9 0 1 6.7E-02 0 0
CUI: C0153380
Disease: Malignant neoplasm of other specified parts of mouth
Malignant neoplasm of other specified parts of mouth 		9 0 1 6.7E-02 0 0
CUI: C0153407
Disease: Malignant neoplasm of other sites within the lip and oral cavity
Malignant neoplasm of other sites within the lip and oral cavity 		9 0 1 6.7E-02 0 0