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: C0268747
Disease: Diffuse mesangial sclerosis (disorder)
Diffuse mesangial sclerosis (disorder) 		22 0 3 0.12 0 0
CUI: C0006902
Disease: Capillaritis
Capillaritis 		3 0 1 0.11 0 0
CUI: C0086588
Disease: Marasmus
Marasmus 		3 0 1 0.11 0 0
CUI: C0344262
Disease: Anterior lenticonus
Anterior lenticonus 		3 0 1 0.11 0 0
CUI: C0344263
Disease: Posterior lenticonus
Posterior lenticonus 		3 0 1 0.11 0 0
CUI: C1303009
Disease: Microcoria, congenital
Microcoria, congenital 		3 0 1 0.11 0 0
CUI: C1305904
Disease: Familial hematuria
Familial hematuria 		23 0 3 0.11 0 0
CUI: C1739392
Disease: Thin glomerular basement membrane disease
Thin glomerular basement membrane disease 		3 0 1 0.11 0 0
CUI: C1864238
Disease: Prolonged miniature endplate currents
Prolonged miniature endplate currents 		3 0 1 0.11 0 0
CUI: C2931254
Disease: Alport syndrome, recessive type
Alport syndrome, recessive type 		3 0 1 0.11 0 0
CUI: C3276821
Disease: Thin glomerular basement membrane
Thin glomerular basement membrane 		3 0 1 0.11 0 0
CUI: C3278307
Disease: Diffuse glomerular basement membrane lamellation
Diffuse glomerular basement membrane lamellation 		3 0 1 0.11 0 0
CUI: C4746547
Disease: ALPORT SYNDROME 3, AUTOSOMAL DOMINANT
ALPORT SYNDROME 3, AUTOSOMAL DOMINANT 		3 0 1 0.11 0 0
CUI: C0239043
Disease: Difficulty chewing
Difficulty chewing 		14 0 2 0.11 0 0
CUI: C0429494
Disease: Ocular axial length
Ocular axial length 		4 0 1 1.0E-01 0 0
CUI: C0745136
Disease: Hypertensive emergency
Hypertensive emergency 		4 0 1 1.0E-01 0 0
CUI: C0745138
Disease: Hypertensive urgency
Hypertensive urgency 		4 0 1 1.0E-01 0 0
CUI: C1839860
Disease: Elevated amniotic fluid alpha-fetoprotein
Elevated amniotic fluid alpha-fetoprotein 		4 0 1 1.0E-01 0 0
CUI: C1853124
Disease: NEPHROTIC SYNDROME, TYPE 3
NEPHROTIC SYNDROME, TYPE 3 		4 0 1 1.0E-01 0 0
CUI: C1865318
Disease: Abnormality of the temporomandibular joint
Abnormality of the temporomandibular joint 		4 0 1 1.0E-01 0 0
CUI: C4021775
Disease: High-frequency sensorineural hearing impairment
High-frequency sensorineural hearing impairment 		4 0 1 1.0E-01 0 0
CUI: C4022576
Disease: Slow pupillary light response
Slow pupillary light response 		4 0 1 1.0E-01 0 0
CUI: C4746745
Disease: ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE
ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE 		4 0 1 1.0E-01 0 0
CUI: C1862481
Disease: Limited wrist extension
Limited wrist extension 		5 0 1 9.1E-02 0 0
CUI: C4022749
Disease: Abnormal brainstem MRI signal intensity
Abnormal brainstem MRI signal intensity 		5 0 1 9.1E-02 0 0