Source: INFERRED ×
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: C0041296
Disease: Tuberculosis
Tuberculosis 		0 28 0 0 1 1.5E-02
CUI: C4277682
Disease: Chemical and Drug Induced Liver Injury
Chemical and Drug Induced Liver Injury 		0 38 0 0 1 1.3E-02
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		1 9 1 5.3E-02 6 0.14
CUI: C0031941
Disease: Pineal Gland Neoplasm
Pineal Gland Neoplasm 		1 0 1 5.3E-02 0 0
CUI: C0033141
Disease: Cardiomyopathies, Primary
Cardiomyopathies, Primary 		1 0 1 5.3E-02 0 0
CUI: C0238122
Disease: Fallopian Tube Carcinoma
Fallopian Tube Carcinoma 		1 0 1 5.3E-02 0 0
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty 		1 0 1 5.3E-02 0 0
CUI: C0343114
Disease: Woolly hair nevus
Woolly hair nevus 		1 1 1 5.3E-02 1 2.6E-02
CUI: C0346300
Disease: Pituitary carcinoma
Pituitary carcinoma 		1 1 1 5.3E-02 1 2.6E-02
CUI: C0410529
Disease: Hypochondroplasia (disorder)
Hypochondroplasia (disorder) 		1 21 1 5.3E-02 7 0.13
CUI: C0587248
Disease: Costello syndrome (disorder)
Costello syndrome (disorder) 		1 16 1 5.3E-02 3 5.8E-02
CUI: C1300257
Disease: Thanatophoric dysplasia, type 2
Thanatophoric dysplasia, type 2 		1 14 1 5.3E-02 7 0.15
CUI: C1842881
Disease: Dilated aortic root
Dilated aortic root 		1 0 1 5.3E-02 0 0
CUI: C1851152
Disease: SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS
SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS 		1 1 1 5.3E-02 1 2.6E-02
CUI: C1859624
Disease: Defective B cell differentiation
Defective B cell differentiation 		1 0 1 5.3E-02 0 0
CUI: C1861213
Disease: Wide-cupped costochondral junctions
Wide-cupped costochondral junctions 		1 0 1 5.3E-02 0 0
CUI: C1863423
Disease: Lumbar kyphosis in infancy
Lumbar kyphosis in infancy 		1 0 1 5.3E-02 0 0
CUI: C1864436
Disease: Muenke Syndrome
Muenke Syndrome 		1 7 1 5.3E-02 6 0.15
CUI: C1864852
Disease: CATSHL syndrome
CATSHL syndrome 		1 10 1 5.3E-02 6 0.14
CUI: C1864854
Disease: Broad femoral metaphyses
Broad femoral metaphyses 		1 0 1 5.3E-02 0 0
CUI: C1868678
Disease: THANATOPHORIC DYSPLASIA, TYPE I (disorder)
THANATOPHORIC DYSPLASIA, TYPE I (disorder) 		1 12 1 5.3E-02 6 0.13
CUI: C1968782
Disease: MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES
MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES 		1 4 1 5.3E-02 2 4.9E-02
CUI: C2608045
Disease: Trilateral Retinoblastoma
Trilateral Retinoblastoma 		1 0 1 5.3E-02 0 0
CUI: C2674171
Disease: Lethal short-limbed short stature
Lethal short-limbed short stature 		1 1 1 5.3E-02 1 2.6E-02
CUI: C2674173
Disease: Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans 		1 7 1 5.3E-02 6 0.15