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: C0270724
Disease: Infantile Neuroaxonal Dystrophy
Infantile Neuroaxonal Dystrophy 		17 0 8 0.31 0 0
CUI: C3496228
Disease: Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia
Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia 		5 0 4 0.22 0 0
CUI: C4517377
Disease: Coenzyme A synthase protein associated neurodegeneration
Coenzyme A synthase protein associated neurodegeneration 		5 0 4 0.22 0 0
CUI: C0018523
Disease: Hallervorden-Spatz Syndrome
Hallervorden-Spatz Syndrome 		22 0 7 0.22 0 0
CUI: C1847640
Disease: KUFOR-RAKEB SYNDROME
KUFOR-RAKEB SYNDROME 		11 0 5 0.22 0 0
CUI: C3550973
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5 		19 0 6 0.20 0 0
CUI: C2931845
Disease: Neurodegeneration with brain iron accumulation (NBIA)
Neurodegeneration with brain iron accumulation (NBIA) 		40 0 9 0.19 0 0
CUI: C4302857
Disease: Malignancy-associated membranous nephropathy
Malignancy-associated membranous nephropathy 		4 0 3 0.17 0 0
CUI: C0391820
Disease: Gouty nephropathy
Gouty nephropathy 		5 0 3 0.16 0 0
CUI: C4054543
Disease: Membranous Lupus Nephritis
Membranous Lupus Nephritis 		6 0 3 0.15 0 0
CUI: C1260881
Disease: Allergic bronchitis
Allergic bronchitis 		8 0 3 0.14 0 0
CUI: C3711384
Disease: Distal Hereditary Motor Neuropathy, Type II
Distal Hereditary Motor Neuropathy, Type II 		8 0 3 0.14 0 0
CUI: C0342286
Disease: Woodhouse Sakati syndrome
Woodhouse Sakati syndrome 		9 0 3 0.13 0 0
CUI: C1858479
Disease: Spastic paraplegia 11, autosomal recessive
Spastic paraplegia 11, autosomal recessive 		9 0 3 0.13 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 4 0.13 0 0
CUI: C0015371
Disease: Extrapyramidal Disorders
Extrapyramidal Disorders 		27 0 5 0.13 0 0
CUI: C2674616
Disease: FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder)
FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder) 		10 0 3 0.12 0 0
CUI: C1837657
Disease: Spondyloepiphyseal dysplasia, Omani type
Spondyloepiphyseal dysplasia, Omani type 		3 0 2 0.11 0 0
CUI: C4021076
Disease: Iron accumulation in brain
Iron accumulation in brain 		3 0 2 0.11 0 0
CUI: C4022786
Disease: Iron accumulation in globus pallidus
Iron accumulation in globus pallidus 		3 0 2 0.11 0 0
CUI: C1328577
Disease: Empty follicle syndrome
Empty follicle syndrome 		14 0 3 0.11 0 0
CUI: C1142448
Disease: Apraxia of eyelid
Apraxia of eyelid 		5 0 2 1.0E-01 0 0
CUI: C1868251
Disease: Neonatal alloimmune thrombocytopenia (NAIT)
Neonatal alloimmune thrombocytopenia (NAIT) 		6 0 2 9.5E-02 0 0
CUI: C3273225
Disease: Hereditary Neurodegenerative Disorder
Hereditary Neurodegenerative Disorder 		6 0 2 9.5E-02 0 0
CUI: C0751870
Disease: Heredodegenerative Disorders, Nervous System
Heredodegenerative Disorders, Nervous System 		18 0 3 9.4E-02 0 0