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: C0023138
Disease: Laurence-Moon Syndrome
Laurence-Moon Syndrome 		1 0 1 1.7E-02 0 0
CUI: C0034350
Disease: Pyruvate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors 		1 0 1 1.7E-02 0 0
CUI: C0037050
Disease: Sick Building Syndrome
Sick Building Syndrome 		1 0 1 1.7E-02 0 0
CUI: C0155002
Disease: Sudden visual loss
Sudden visual loss 		1 0 1 1.7E-02 0 0
CUI: C0221727
Disease: Pain in esophagus (finding)
Pain in esophagus (finding) 		1 0 1 1.7E-02 0 0
CUI: C0423640
Disease: Right Flank Pain
Right Flank Pain 		1 0 1 1.7E-02 0 0
CUI: C1739147
Disease: Subacute necrotising encephalomyopathy
Subacute necrotising encephalomyopathy 		1 0 1 1.7E-02 0 0
CUI: C1835896
Disease: SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder) 		1 0 1 1.7E-02 0 0
CUI: C1838868
Disease: Corticospinal tract atrophy
Corticospinal tract atrophy 		1 0 1 1.7E-02 0 0
CUI: C1838916
Disease: ATAXIA AND POLYNEUROPATHY, ADULT-ONSET
ATAXIA AND POLYNEUROPATHY, ADULT-ONSET 		1 0 1 1.7E-02 0 0
CUI: C1839022
Disease: Striatonigral Degeneration, Infantile, Mitochondrial
Striatonigral Degeneration, Infantile, Mitochondrial 		1 0 1 1.7E-02 0 0
CUI: C1845243
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE 		1 0 1 1.7E-02 0 0
CUI: C1848735
Disease: Developmental delay, mild
Developmental delay, mild 		1 0 1 1.7E-02 0 0
CUI: C1850395
Disease: Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive
Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive 		1 0 1 1.7E-02 0 0
CUI: C1859093
Disease: Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism 		1 0 1 1.7E-02 0 0
CUI: C1864929
Disease: Cerebellar atrophy, progressive
Cerebellar atrophy, progressive 		1 0 1 1.7E-02 0 0
CUI: C1968811
Disease: Prominent antitragus
Prominent antitragus 		1 0 1 1.7E-02 0 0
CUI: C1968814
Disease: Slender ulna
Slender ulna 		1 0 1 1.7E-02 0 0
CUI: C2675528
Disease: Spastic Paraplegia 42, Autosomal Dominant
Spastic Paraplegia 42, Autosomal Dominant 		1 0 1 1.7E-02 0 0
CUI: C2677586
Disease: Spastic Paraplegia 39, Autosomal Recessive
Spastic Paraplegia 39, Autosomal Recessive 		1 0 1 1.7E-02 0 0
CUI: C3150898
Disease: CARDIOMYOPATHY, DILATED, 1GG
CARDIOMYOPATHY, DILATED, 1GG 		1 0 1 1.7E-02 0 0
CUI: C3150901
Disease: SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE 		1 0 1 1.7E-02 0 0
CUI: C3275684
Disease: MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1 		1 0 1 1.7E-02 0 0
CUI: C3279992
Disease: PARAGANGLIOMAS 5
PARAGANGLIOMAS 5 		1 0 1 1.7E-02 0 0
CUI: C3280168
Disease: NEUROPATHY, HEREDITARY SENSORY, TYPE IIC
NEUROPATHY, HEREDITARY SENSORY, TYPE IIC 		1 0 1 1.7E-02 0 0