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: C4021986
Disease: Hypoplasia of the ear cartilage
Hypoplasia of the ear cartilage 		14 0 8 0.38 0 0
CUI: C4025249
Disease: Abnormality of the intervertebral disk
Abnormality of the intervertebral disk 		30 0 8 0.22 0 0
CUI: C2936786
Disease: Aqueductal Stenosis
Aqueductal Stenosis 		34 0 8 0.20 0 0
CUI: C0268747
Disease: Diffuse mesangial sclerosis (disorder)
Diffuse mesangial sclerosis (disorder) 		22 0 6 0.19 0 0
CUI: C3489393
Disease: Hiatal Hernia
Hiatal Hernia 		39 0 8 0.17 0 0
CUI: C4023616
Disease: Abnormality of immune system physiology
Abnormality of immune system physiology 		42 0 8 0.16 0 0
CUI: C1847114
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5 		2 0 2 0.13 0 0
CUI: C4551772
Disease: GALLOWAY-MOWAT SYNDROME 1
GALLOWAY-MOWAT SYNDROME 1 		3 0 2 0.12 0 0
CUI: C0403397
Disease: Steroid-resistant nephrotic syndrome
Steroid-resistant nephrotic syndrome 		73 0 9 0.11 0 0
CUI: C3266102
Disease: Steroid resistant nephrotic syndrome of childhood
Steroid resistant nephrotic syndrome of childhood 		73 0 9 0.11 0 0
CUI: C1704320
Disease: Glomerulonephritis, Minimal Change
Glomerulonephritis, Minimal Change 		7 0 2 1.0E-01 0 0
CUI: C3554617
Disease: Adducted thumb
Adducted thumb 		74 0 8 9.9E-02 0 0
CUI: C2748610
Disease: Progressive extrapyramidal movement disorder
Progressive extrapyramidal movement disorder 		9 0 2 9.1E-02 0 0
CUI: C2749515
Disease: Collapsing glomerulopathy
Collapsing glomerulopathy 		10 0 2 8.7E-02 0 0
CUI: C1305904
Disease: Familial hematuria
Familial hematuria 		23 0 3 8.6E-02 0 0
CUI: C0424711
Disease: Orbital separation diminished
Orbital separation diminished 		89 0 8 8.3E-02 0 0
CUI: C4511620
Disease: Autosomal dominant tubulointerstitial kidney disease
Autosomal dominant tubulointerstitial kidney disease 		13 0 2 7.7E-02 0 0
CUI: C1868672
Disease: NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE
NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE 		31 0 3 7.0E-02 0 0
CUI: C0375206
Disease: Hemiplegia/hemiparesis
Hemiplegia/hemiparesis 		112 0 8 6.7E-02 0 0
CUI: C0333494
Disease: Phlebosclerosis
Phlebosclerosis 		1 0 1 6.7E-02 0 0
CUI: C0549315
Disease: Hydatidiform mole, benign
Hydatidiform mole, benign 		1 0 1 6.7E-02 0 0
CUI: C1836890
Disease: Hypoplasia of the ciliary body
Hypoplasia of the ciliary body 		1 0 1 6.7E-02 0 0
CUI: C1858395
Disease: Tubular atrophy
Tubular atrophy 		17 0 2 6.7E-02 0 0
CUI: C3280113
Disease: NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES
NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES 		1 0 1 6.7E-02 0 0
CUI: C3489732
Disease: Familial mesangial sclerosis
Familial mesangial sclerosis 		1 0 1 6.7E-02 0 0