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: C4021774
Disease: Camptodactyly of toe
Camptodactyly of toe 		9 0 1 0.11 0 0
CUI: C1851542
Disease: Limited hip movement
Limited hip movement 		10 0 1 1.0E-01 0 0
CUI: C4021742
Disease: Abnormality of the humerus
Abnormality of the humerus 		10 0 1 1.0E-01 0 0
CUI: C1837761
Disease: Narrow nasal ridge
Narrow nasal ridge 		11 0 1 9.1E-02 0 0
CUI: C4048199
Disease: Ulnar deviation of the hand or of fingers of the hand
Ulnar deviation of the hand or of fingers of the hand 		11 0 1 9.1E-02 0 0
CUI: C3151520
Disease: Early severe fetal akinesia sequence
Early severe fetal akinesia sequence 		12 0 1 8.3E-02 0 0
CUI: C0422895
Disease: Primitive reflex
Primitive reflex 		14 0 1 7.1E-02 0 0
CUI: C1838319
Disease: Primitive reflexes (palmomental, snout, glabellar)
Primitive reflexes (palmomental, snout, glabellar) 		14 0 1 7.1E-02 0 0
CUI: C0220666
Disease: ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA
ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA 		15 0 1 6.7E-02 0 0
CUI: C0240914
Disease: Romberg's sign positive
Romberg's sign positive 		15 0 1 6.7E-02 0 0
CUI: C1837835
Disease: Bilateral talipes equinovarus
Bilateral talipes equinovarus 		16 0 1 6.2E-02 0 0
CUI: C4025763
Disease: Abnormality of the rib cage
Abnormality of the rib cage 		16 0 1 6.2E-02 0 0
CUI: C4317152
Disease: Dimple chin
Dimple chin 		16 0 1 6.2E-02 0 0
CUI: C4023681
Disease: Delayed fine motor development
Delayed fine motor development 		19 0 1 5.3E-02 0 0
CUI: C4025773
Disease: Aplasia/Hypoplasia involving the skeletal musculature
Aplasia/Hypoplasia involving the skeletal musculature 		19 0 1 5.3E-02 0 0
CUI: C0043515
Disease: Zollinger-Ellison syndrome
Zollinger-Ellison syndrome 		20 0 1 5.0E-02 0 0
CUI: C0749379
Disease: Thoracolumbar scoliosis
Thoracolumbar scoliosis 		20 0 1 5.0E-02 0 0
CUI: C4021254
Disease: Cutaneous finger syndactyly
Cutaneous finger syndactyly 		20 0 1 5.0E-02 0 0
CUI: C1704421
Disease: Skin Pigmentation Disorder
Skin Pigmentation Disorder 		21 0 1 4.8E-02 0 0
CUI: C0265213
Disease: Distal arthrogryposis syndrome
Distal arthrogryposis syndrome 		22 0 1 4.5E-02 0 0
CUI: C1842587
Disease: Sensory axonal neuropathy
Sensory axonal neuropathy 		23 0 1 4.3E-02 0 0
CUI: C1834523
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 2B
ARTHROGRYPOSIS, DISTAL, TYPE 2B 		25 0 1 4.0E-02 0 0
CUI: C3150077
Disease: Mild short stature
Mild short stature 		25 0 1 4.0E-02 0 0
CUI: C1449844
Disease: Pseudohypoaldosteronism, Type II
Pseudohypoaldosteronism, Type II 		27 0 1 3.7E-02 0 0
CUI: C1698196
Disease: Muscle Weakness Upper Limb
Muscle Weakness Upper Limb 		29 0 1 3.4E-02 0 0