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: C1857482
Disease: Slender finger
Slender finger 		20 0 1 5.0E-02 0 0
CUI: C3163798
Disease: Recurrent lower respiratory tract infection
Recurrent lower respiratory tract infection 		23 0 1 4.3E-02 0 0
CUI: C3150613
Disease: Long toe
Long toe 		24 0 1 4.2E-02 0 0
CUI: C1578482
Disease: Valgus deformities of feet
Valgus deformities of feet 		26 0 1 3.8E-02 0 0
CUI: C4316810
Disease: Writer's Cramp
Writer's Cramp 		26 0 1 3.8E-02 0 0
CUI: C0393588
Disease: Dystonia, Paroxysmal
Dystonia, Paroxysmal 		28 0 1 3.6E-02 0 0
CUI: C1836156
Disease: Progressive proximal muscle weakness
Progressive proximal muscle weakness 		28 0 1 3.6E-02 0 0
CUI: C1850794
Disease: Proximal amyotrophy
Proximal amyotrophy 		29 0 1 3.4E-02 0 0
CUI: C0263383
Disease: Keratosis pilaris
Keratosis pilaris 		30 0 1 3.3E-02 0 0
CUI: C1850573
Disease: Slender build
Slender build 		31 0 1 3.2E-02 0 0
CUI: C2930471
Disease: Bilateral Wilms Tumor
Bilateral Wilms Tumor 		31 0 1 3.2E-02 0 0
CUI: C0206647
Disease: Dermatofibrosarcoma
Dermatofibrosarcoma 		33 0 1 3.0E-02 0 0
CUI: C4021815
Disease: Abnormal palate morphology
Abnormal palate morphology 		40 0 1 2.5E-02 0 0
CUI: C1858127
Disease: Limb-girdle muscle weakness
Limb-girdle muscle weakness 		41 0 1 2.4E-02 0 0
CUI: C0751093
Disease: Dystonia, Limb
Dystonia, Limb 		42 0 1 2.4E-02 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 1 2.3E-02 0 0
CUI: C1852502
Disease: CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT 		45 0 1 2.2E-02 0 0
CUI: C2827469
Disease: Coronary Microvascular Disease
Coronary Microvascular Disease 		45 0 1 2.2E-02 0 0
CUI: C0431129
Disease: Adamantinous Craniopharyngioma
Adamantinous Craniopharyngioma 		48 0 1 2.1E-02 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 1 2.0E-02 0 0
CUI: C0699743
Disease: Congenital muscular dystrophy (disorder)
Congenital muscular dystrophy (disorder) 		54 0 1 1.9E-02 0 0
CUI: C0040485
Disease: Torticollis
Torticollis 		55 0 1 1.8E-02 0 0
CUI: C1858025
Disease: Spinal rigidity
Spinal rigidity 		55 0 1 1.8E-02 0 0
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy 		56 0 1 1.8E-02 0 0
CUI: C0234378
Disease: Static Tremor
Static Tremor 		62 0 1 1.6E-02 0 0