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: C0269014
Disease: Fibrosis of corpus cavernosum
Fibrosis of corpus cavernosum
1 0 1 0.50 0 0
CUI: C0857856
Disease: Staphylococcus aureus abscess
Staphylococcus aureus abscess
1 0 1 0.50 0 0
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
1 0 1 0.50 0 0
CUI: C2711256
Disease: Ischemic priapism
Ischemic priapism
1 0 1 0.50 0 0
CUI: C4225268
Disease: CUTIS LAXA, AUTOSOMAL DOMINANT 3
CUTIS LAXA, AUTOSOMAL DOMINANT 3
1 0 1 0.50 0 0
SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE
1 0 1 0.50 0 0
CUI: C0268341
Disease: Ehlers-Danlos syndrome type 5
Ehlers-Danlos syndrome type 5
2 0 1 0.33 0 0
CUI: C0268354
Disease: De Barsy syndrome
De Barsy syndrome
2 0 1 0.33 0 0
Malignant neoplasm of stomach stage II
2 0 1 0.33 0 0
CUI: C0392477
Disease: Congenital flat foot
Congenital flat foot
2 0 1 0.33 0 0
CUI: C0740268
Disease: Pelvic prolapse
Pelvic prolapse
2 0 1 0.33 0 0
SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder)
2 0 1 0.33 0 0
Cutis Laxa, Autosomal Recessive, Type IIB
2 0 1 0.33 0 0
Abnormality of the dorsal column of the spinal cord
2 0 1 0.33 0 0
AORTIC ANEURYSM, FAMILIAL THORACIC 10
2 0 1 0.33 0 0
CUI: C4476943
Disease: Impaired continence
Impaired continence
2 0 1 0.33 0 0
CUI: C0018245
Disease: Groenouw's Dystrophies
Groenouw's Dystrophies
3 0 1 0.25 0 0
CUI: C0268350
Disease: Cutis Laxa, Autosomal Dominant
Cutis Laxa, Autosomal Dominant
3 0 1 0.25 0 0
CUI: C0748012
Disease: Nodular prostate
Nodular prostate
3 0 1 0.25 0 0
CUI: C1144799
Disease: Hypertensive cardiomyopathy
Hypertensive cardiomyopathy
3 0 1 0.25 0 0
Atrophy of quadriceps femoris muscle
3 0 1 0.25 0 0
Non-Alzheimer's dementia (e.g., Lewy body dementia, vascular or multi-infarct dementia; mixed dementia; frontotemporal dementia such as Pick's disease; and dementia related to stroke, Parkinson's or Creutzfeldt-Jakob diseases)
3 0 1 0.25 0 0
CUI: C0264133
Disease: Acquired flat foot
Acquired flat foot
4 0 1 0.20 0 0
Dysfunction of lateral corticospinal tracts
4 0 1 0.20 0 0
CUI: C1848771
Disease: Prominent superficial blood vessels
Prominent superficial blood vessels
4 0 1 0.20 0 0