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: C4021572
Disease: Excessive wrinkling of palmar skin
Excessive wrinkling of palmar skin 		2 0 1 8.3E-02 0 0
CUI: C4310232
Disease: Hypercalcemia, Infantile, 1
Hypercalcemia, Infantile, 1 		2 0 1 8.3E-02 0 0
CUI: C4310473
Disease: Hypercalcemia, infantile, 2
Hypercalcemia, infantile, 2 		2 0 1 8.3E-02 0 0
CUI: C4330845
Disease: Nutritional Rickets
Nutritional Rickets 		2 0 1 8.3E-02 0 0
CUI: C4551503
Disease: FANCONI RENOTUBULAR SYNDROME 1
FANCONI RENOTUBULAR SYNDROME 1 		2 0 1 8.3E-02 0 0
CUI: C0268080
Disease: Hypercalcemia, Idiopathic, of Infancy
Hypercalcemia, Idiopathic, of Infancy 		3 0 1 7.7E-02 0 0
CUI: C0409860
Disease: Rotator cuff tear arthropathy
Rotator cuff tear arthropathy 		3 0 1 7.7E-02 0 0
CUI: C0410719
Disease: Deformity of bone
Deformity of bone 		17 0 2 7.7E-02 0 0
CUI: C0518988
Disease: Dental abscess
Dental abscess 		3 0 1 7.7E-02 0 0
CUI: C1853271
Disease: HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY
HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY 		3 0 1 7.7E-02 0 0
CUI: C1969738
Disease: Premature loss of permanent teeth
Premature loss of permanent teeth 		3 0 1 7.7E-02 0 0
CUI: C0002957
Disease: Anger
Anger 		4 0 1 7.1E-02 0 0
CUI: C0156257
Disease: Calculus of kidney and ureter
Calculus of kidney and ureter 		4 0 1 7.1E-02 0 0
CUI: C0241932
Disease: X-linked hypogammaglobulinemia
X-linked hypogammaglobulinemia 		4 0 1 7.1E-02 0 0
CUI: C1838440
Disease: ICHTHYOSIS EXFOLIATIVA
ICHTHYOSIS EXFOLIATIVA 		4 0 1 7.1E-02 0 0
CUI: C1839612
Disease: MYOPIA 1, X-LINKED
MYOPIA 1, X-LINKED 		4 0 1 7.1E-02 0 0
CUI: C1853354
Disease: Peeling skin syndrome, acral type
Peeling skin syndrome, acral type 		4 0 1 7.1E-02 0 0
CUI: C1859133
Disease: RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1
RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1 		4 0 1 7.1E-02 0 0
CUI: C1860130
Disease: Low alkaline phosphatase
Low alkaline phosphatase 		4 0 1 7.1E-02 0 0
CUI: C2919414
Disease: Low density lipoprotein receptor mutation
Low density lipoprotein receptor mutation 		4 0 1 7.1E-02 0 0
CUI: C4727947
Disease: Hypophosphataemic osteomalacia
Hypophosphataemic osteomalacia 		4 0 1 7.1E-02 0 0
CUI: C0202251
Disease: Vitamin B6 measurement
Vitamin B6 measurement 		5 11 1 6.7E-02 2 7.7E-02
CUI: C0342749
Disease: GLYCOGEN STORAGE DISEASE Ic
GLYCOGEN STORAGE DISEASE Ic 		5 0 1 6.7E-02 0 0
CUI: C0475732
Disease: Hypercalcemia, Infantile
Hypercalcemia, Infantile 		5 0 1 6.7E-02 0 0
CUI: C1443296
Disease: Axial myopia
Axial myopia 		5 0 1 6.7E-02 0 0