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: C4023610
Disease: Abnormality of the intrinsic pathway
Abnormality of the intrinsic pathway 		4 0 1 0.20 0 0
CUI: C4024871
Disease: Prominent veins on trunk
Prominent veins on trunk 		4 0 1 0.20 0 0
CUI: C4024970
Disease: Thick cerebral cortex
Thick cerebral cortex 		4 0 1 0.20 0 0
CUI: C4476632
Disease: Fragmented elastic fibers in the dermis
Fragmented elastic fibers in the dermis 		4 0 1 0.20 0 0
CUI: C0432255
Disease: Geroderma osteodysplastica
Geroderma osteodysplastica 		5 0 1 0.17 0 0
CUI: C1299493
Disease: Developmental failure of fusion
Developmental failure of fusion 		5 0 1 0.17 0 0
CUI: C3714535
Disease: Malocclusion, Angle class II
Malocclusion, Angle class II 		5 0 1 0.17 0 0
CUI: C3874346
Disease: Skeletal malocclusion
Skeletal malocclusion 		5 0 1 0.17 0 0
CUI: C0240414
Disease: Hypoplasia of muscle
Hypoplasia of muscle 		6 0 1 0.14 0 0
CUI: C1856714
Disease: Palmoplantar cutis laxa
Palmoplantar cutis laxa 		6 0 1 0.14 0 0
CUI: C1866487
Disease: Prominent nasolabial fold
Prominent nasolabial fold 		6 0 1 0.14 0 0
CUI: C2861614
Disease: AML M5b
AML M5b 		6 0 1 0.14 0 0
CUI: C0266283
Disease: Ectopic thyroid tissue (disorder)
Ectopic thyroid tissue (disorder) 		8 0 1 0.11 0 0
CUI: C0342286
Disease: Woodhouse Sakati syndrome
Woodhouse Sakati syndrome 		9 0 1 1.0E-01 0 0
CUI: C1303003
Disease: Epicanthus inversus
Epicanthus inversus 		9 0 1 1.0E-01 0 0
CUI: C1859347
Disease: Abnormal subcutaneous fat tissue distribution
Abnormal subcutaneous fat tissue distribution 		9 0 1 1.0E-01 0 0
CUI: C0332915
Disease: Congenital failure of fusion
Congenital failure of fusion 		11 0 1 8.3E-02 0 0
CUI: C0423808
Disease: Brachyonychia
Brachyonychia 		11 0 1 8.3E-02 0 0
CUI: C0749420
Disease: Thyroid Agenesis
Thyroid Agenesis 		11 0 1 8.3E-02 0 0
CUI: C1318518
Disease: Infantile malignant osteopetrosis
Infantile malignant osteopetrosis 		13 0 1 7.1E-02 0 0
CUI: C1836842
Disease: Psychomotor deterioration
Psychomotor deterioration 		13 0 1 7.1E-02 0 0
CUI: C0151516
Disease: Thyroid Hypoplasia
Thyroid Hypoplasia 		14 0 1 6.7E-02 0 0
CUI: C1859447
Disease: Hypoplastic ischia
Hypoplastic ischia 		14 0 1 6.7E-02 0 0
CUI: C2749688
Disease: Abnormal isoelectric focusing of serum transferrin
Abnormal isoelectric focusing of serum transferrin 		15 0 1 6.2E-02 0 0
CUI: C1840319
Disease: Redundant neck skin
Redundant neck skin 		16 0 1 5.9E-02 0 0