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: C0038018
Disease: Spondylolysis
Spondylolysis 		9 0 3 0.14 0 0
CUI: C4022909
Disease: Excessive femoral anteversion
Excessive femoral anteversion 		2 0 2 0.12 0 0
CUI: C0410740
Disease: Acquired deformity of finger
Acquired deformity of finger 		5 0 2 0.11 0 0
CUI: C0019555
Disease: Hip Dislocation, Congenital
Hip Dislocation, Congenital 		6 0 2 1.0E-01 0 0
CUI: C4551566
Disease: Equinovarus deformity of foot
Equinovarus deformity of foot 		6 0 2 1.0E-01 0 0
CUI: C0282102
Disease: Chondrodysplasia punctata, X-linked dominant type
Chondrodysplasia punctata, X-linked dominant type 		9 0 2 8.7E-02 0 0
CUI: C3887531
Disease: Keratoglobus
Keratoglobus 		9 0 2 8.7E-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 2 8.0E-02 0 0
CUI: C0266050
Disease: Failure of exfoliation of primary tooth
Failure of exfoliation of primary tooth 		12 1 2 7.7E-02 1 0.17
CUI: C1578482
Disease: Valgus deformities of feet
Valgus deformities of feet 		26 0 3 7.7E-02 0 0
CUI: C1842229
Disease: Broad metacarpals
Broad metacarpals 		12 0 2 7.7E-02 0 0
CUI: C4082169
Disease: Metatarsus Varus
Metatarsus Varus 		41 0 4 7.5E-02 0 0
CUI: C4021390
Disease: Symphalangism affecting the phalanges of the hand
Symphalangism affecting the phalanges of the hand 		13 0 2 7.4E-02 0 0
CUI: C0008445
Disease: Chondrodysplasia Punctata
Chondrodysplasia Punctata 		16 0 2 6.7E-02 0 0
CUI: C4317152
Disease: Dimple chin
Dimple chin 		16 0 2 6.7E-02 0 0
CUI: C0239181
Disease: Intermittent diarrhea
Intermittent diarrhea 		17 0 2 6.5E-02 0 0
CUI: C0019295
Disease: Inguinal Hernia, Direct
Inguinal Hernia, Direct 		1 0 1 6.2E-02 0 0
CUI: C0153614
Disease: Malignant neoplasm of ureteric orifice
Malignant neoplasm of ureteric orifice 		1 0 1 6.2E-02 0 0
CUI: C0270149
Disease: Perinatal respiratory distress
Perinatal respiratory distress 		1 0 1 6.2E-02 0 0
CUI: C0333662
Disease: Hemiatrophy
Hemiatrophy 		1 0 1 6.2E-02 0 0
CUI: C0423729
Disease: Chest pain on breathing
Chest pain on breathing 		1 0 1 6.2E-02 0 0
CUI: C0796159
Disease: Mental retardation Smith Fineman Myers type
Mental retardation Smith Fineman Myers type 		1 0 1 6.2E-02 0 0
CUI: C0854486
Disease: Secretory adenoma of pituitary
Secretory adenoma of pituitary 		1 0 1 6.2E-02 0 0
CUI: C1112616
Disease: Loss of proprioception
Loss of proprioception 		1 0 1 6.2E-02 0 0
CUI: C1300285
Disease: SAUL-WILSON SYNDROME
SAUL-WILSON SYNDROME 		1 1 1 6.2E-02 1 0.17