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: C3825926
Disease: Nephrotic syndrome in children
Nephrotic syndrome in children 		6 0 2 0.18 0 0
CUI: C0445118
Disease: Nephrotic range proteinuria
Nephrotic range proteinuria 		7 0 2 0.17 0 0
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome 		7 0 2 0.17 0 0
CUI: C0887976
Disease: Chlamydophila Infections
Chlamydophila Infections 		1 0 1 0.14 0 0
CUI: C3280103
Disease: Podocyte foot process effacement
Podocyte foot process effacement 		1 0 1 0.14 0 0
CUI: C3554634
Disease: Light complexion
Light complexion 		1 0 1 0.14 0 0
CUI: C4014507
Disease: NEPHROTIC SYNDROME, TYPE 10
NEPHROTIC SYNDROME, TYPE 10 		1 0 1 0.14 0 0
CUI: C4073167
Disease: Osteolysis involving bones of the upper limbs
Osteolysis involving bones of the upper limbs 		1 0 1 0.14 0 0
CUI: C4225228
Disease: NEPHROTIC SYNDROME, TYPE 11
NEPHROTIC SYNDROME, TYPE 11 		1 0 1 0.14 0 0
CUI: C4538784
Disease: GALLOWAY-MOWAT SYNDROME 2, X-LINKED
GALLOWAY-MOWAT SYNDROME 2, X-LINKED 		1 0 1 0.14 0 0
CUI: C4748084
Disease: OVARIAN DYSGENESIS 6
OVARIAN DYSGENESIS 6 		1 0 1 0.14 0 0
CUI: C0403399
Disease: Finnish congenital nephrotic syndrome
Finnish congenital nephrotic syndrome 		11 0 2 0.12 0 0
CUI: C0432289
Disease: Winchester syndrome (disorder)
Winchester syndrome (disorder) 		2 0 1 0.12 0 0
CUI: C4016901
Disease: NEPHROTIC SYNDROME, TYPE 2, SUSCEPTIBILITY TO
NEPHROTIC SYNDROME, TYPE 2, SUSCEPTIBILITY TO 		2 0 1 0.12 0 0
CUI: C4024579
Disease: Osteolysis involving bones of the feet
Osteolysis involving bones of the feet 		2 0 1 0.12 0 0
CUI: C4025195
Disease: Sclerotic cranial sutures
Sclerotic cranial sutures 		2 0 1 0.12 0 0
CUI: C4539896
Disease: NEPHROTIC SYNDROME, TYPE 15
NEPHROTIC SYNDROME, TYPE 15 		2 0 1 0.12 0 0
CUI: C1868672
Disease: NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE
NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE 		31 0 4 0.12 0 0
CUI: C0268747
Disease: Diffuse mesangial sclerosis (disorder)
Diffuse mesangial sclerosis (disorder) 		22 0 3 0.12 0 0
CUI: C1333843
Disease: Grade 3 Invasive Breast Carcinoma
Grade 3 Invasive Breast Carcinoma 		3 0 1 0.11 0 0
CUI: C1833734
Disease: Carpal osteolysis
Carpal osteolysis 		3 0 1 0.11 0 0
CUI: C1833735
Disease: Osteolysis involving tarsal bones
Osteolysis involving tarsal bones 		3 0 1 0.11 0 0
CUI: C4511620
Disease: Autosomal dominant tubulointerstitial kidney disease
Autosomal dominant tubulointerstitial kidney disease 		13 0 2 0.11 0 0
CUI: C4021986
Disease: Hypoplasia of the ear cartilage
Hypoplasia of the ear cartilage 		14 0 2 0.11 0 0
CUI: C0795949
Disease: Galloway Mowat syndrome
Galloway Mowat syndrome 		15 0 2 1.0E-01 0 0