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 10 0.34 0 0
CUI: C1846582
Disease: Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration 		7 5 7 0.32 4 9.3E-02
CUI: C1847640
Disease: KUFOR-RAKEB SYNDROME
KUFOR-RAKEB SYNDROME 		11 0 6 0.22 0 0
CUI: C1853578
Disease: Neuroferritinopathy
Neuroferritinopathy 		17 0 7 0.22 0 0
CUI: C0877024
Disease: Schimke immunoosseous dysplasia
Schimke immunoosseous dysplasia 		21 0 7 0.19 0 0
CUI: C4517377
Disease: Coenzyme A synthase protein associated neurodegeneration
Coenzyme A synthase protein associated neurodegeneration 		5 0 4 0.17 0 0
CUI: C3550973
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5 		19 0 6 0.17 0 0
CUI: C2931845
Disease: Neurodegeneration with brain iron accumulation (NBIA)
Neurodegeneration with brain iron accumulation (NBIA) 		40 0 9 0.17 0 0
CUI: C0264162
Disease: Camptocormia
Camptocormia 		8 0 4 0.15 0 0
CUI: C0342286
Disease: Woodhouse Sakati syndrome
Woodhouse Sakati syndrome 		9 0 4 0.15 0 0
CUI: C0015371
Disease: Extrapyramidal Disorders
Extrapyramidal Disorders 		27 0 6 0.14 0 0
CUI: C4302857
Disease: Malignancy-associated membranous nephropathy
Malignancy-associated membranous nephropathy 		4 0 3 0.13 0 0
CUI: C0813217
Disease: Expressionless face
Expressionless face 		31 0 6 0.13 0 0
CUI: C0391820
Disease: Gouty nephropathy
Gouty nephropathy 		5 0 3 0.12 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 3 0.12 0 0
CUI: C4054543
Disease: Membranous Lupus Nephritis
Membranous Lupus Nephritis 		6 0 3 0.12 0 0
CUI: C0338473
Disease: Neuroaxonal Dystrophies
Neuroaxonal Dystrophies 		7 0 3 0.12 0 0
CUI: C1850100
Disease: PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder)
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder) 		7 0 3 0.12 0 0
CUI: C1260881
Disease: Allergic bronchitis
Allergic bronchitis 		8 0 3 0.11 0 0
CUI: C3711384
Disease: Distal Hereditary Motor Neuropathy, Type II
Distal Hereditary Motor Neuropathy, Type II 		8 0 3 0.11 0 0
CUI: C1858479
Disease: Spastic paraplegia 11, autosomal recessive
Spastic paraplegia 11, autosomal recessive 		9 0 3 0.11 0 0
CUI: C2674616
Disease: FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder)
FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder) 		10 0 3 0.10 0 0
CUI: C0018522
Disease: Hallermann's Syndrome
Hallermann's Syndrome 		13 0 3 9.4E-02 0 0
CUI: C0454600
Disease: Extrapyramidal dysarthria
Extrapyramidal dysarthria 		2 0 2 9.1E-02 0 0
CUI: C0586392
Disease: Parkinsonian tremor
Parkinsonian tremor 		2 0 2 9.1E-02 0 0