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: C0751717
Disease: Juvenile Neuroaxonal Dystrophy
Juvenile Neuroaxonal Dystrophy 		2 0 2 1.00 0 0
CUI: C0751718
Disease: Late Infantile Neuroaxonal Dystrophy
Late Infantile Neuroaxonal Dystrophy 		2 0 2 1.00 0 0
CUI: C1836522
Disease: Schindler Disease, Type II
Schindler Disease, Type II 		1 0 1 0.50 0 0
CUI: C1836525
Disease: White mater abnormalities in the posterior periventricular region
White mater abnormalities in the posterior periventricular region 		1 0 1 0.50 0 0
CUI: C1836544
Disease: Schindler Disease, Type I
Schindler Disease, Type I 		1 0 1 0.50 0 0
CUI: C1836545
Disease: Schindler Disease, Type III
Schindler Disease, Type III 		1 0 1 0.50 0 0
CUI: C3542549
Disease: SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE 		1 0 1 0.50 0 0
CUI: C4024882
Disease: Telangiectasia of the oral mucosa
Telangiectasia of the oral mucosa 		1 0 1 0.50 0 0
CUI: C1836533
Disease: Increased urinary O-linked sialopeptides
Increased urinary O-linked sialopeptides 		2 0 1 0.33 0 0
CUI: C0338473
Disease: Neuroaxonal Dystrophies
Neuroaxonal Dystrophies 		7 0 2 0.29 0 0
CUI: C1857697
Disease: Lip telangiectasia
Lip telangiectasia 		4 0 1 0.20 0 0
CUI: C0751605
Disease: X-Linked, Spastic Paraplegia, Hereditary
X-Linked, Spastic Paraplegia, Hereditary 		5 0 1 0.17 0 0
CUI: C4721916
Disease: HMSN Type V
HMSN Type V 		7 0 1 0.12 0 0
CUI: C0270724
Disease: Infantile Neuroaxonal Dystrophy
Infantile Neuroaxonal Dystrophy 		17 0 2 0.12 0 0
CUI: C1836527
Disease: Distal sensory impairment of all modalities
Distal sensory impairment of all modalities 		9 0 1 1.0E-01 0 0
CUI: C0751604
Disease: Hereditary X-Linked Recessive Spastic Paraplegia
Hereditary X-Linked Recessive Spastic Paraplegia 		10 0 1 9.1E-02 0 0
CUI: C0040921
Disease: Trichomonas Infections
Trichomonas Infections 		14 0 1 6.7E-02 0 0
CUI: C1853959
Disease: Birdshot chorioretinopathy
Birdshot chorioretinopathy 		15 0 1 6.2E-02 0 0
CUI: C1837496
Disease: Axonal degeneration
Axonal degeneration 		17 0 1 5.6E-02 0 0
CUI: C0751603
Disease: Autosomal Recessive Hereditary Spastic Paraplegia
Autosomal Recessive Hereditary Spastic Paraplegia 		20 0 1 4.8E-02 0 0
CUI: C1850601
Disease: Abnormality of brainstem morphology
Abnormality of brainstem morphology 		21 0 1 4.5E-02 0 0
CUI: C0018523
Disease: Hallervorden-Spatz Syndrome
Hallervorden-Spatz Syndrome 		22 0 1 4.3E-02 0 0
CUI: C1853638
Disease: Broad neck
Broad neck 		22 0 1 4.3E-02 0 0
CUI: C0751602
Disease: Hereditary Autosomal Dominant Spastic Paraplegia
Hereditary Autosomal Dominant Spastic Paraplegia 		27 0 1 3.6E-02 0 0
CUI: C0259749
Disease: Autonomic neuropathy
Autonomic neuropathy 		29 0 1 3.3E-02 0 0