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: C3553947
Disease: PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER) 		1 23 1 1.00 23 0.88
CUI: C1864399
Disease: Peroxisome Biogenesis Disorder, Complementation Group 7
Peroxisome Biogenesis Disorder, Complementation Group 7 		2 4 1 0.50 3 0.11
CUI: C3550234
Disease: PEROXISOME BIOGENESIS DISORDER 2B
PEROXISOME BIOGENESIS DISORDER 2B 		5 0 1 0.20 0 0
CUI: C0476217
Disease: Head movements abnormal
Head movements abnormal 		8 0 1 0.12 0 0
CUI: C4721541
Disease: PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) 		11 0 1 9.1E-02 0 0
CUI: C0751594
Disease: Zellweger-Like Syndrome
Zellweger-Like Syndrome 		13 0 1 7.7E-02 0 0
CUI: C1303007
Disease: Brushfield spots
Brushfield spots 		14 0 1 7.1E-02 0 0
CUI: C3279397
Disease: Very long chain fatty acid accumulation
Very long chain fatty acid accumulation 		15 0 1 6.7E-02 0 0
CUI: C4023786
Disease: Elevated levels of phytanic acid
Elevated levels of phytanic acid 		15 0 1 6.7E-02 0 0
CUI: C0431384
Disease: Colpocephaly
Colpocephaly 		17 0 1 5.9E-02 0 0
CUI: C1854699
Disease: Diffuse cerebellar atrophy
Diffuse cerebellar atrophy 		17 0 1 5.9E-02 0 0
CUI: C0282525
Disease: Adrenoleukodystrophy, Neonatal
Adrenoleukodystrophy, Neonatal 		18 0 1 5.6E-02 0 0
CUI: C0282527
Disease: Infantile Refsum Disease (disorder)
Infantile Refsum Disease (disorder) 		18 0 1 5.6E-02 0 0
CUI: C1836392
Disease: Dysmetric saccades
Dysmetric saccades 		18 0 1 5.6E-02 0 0
CUI: C1845123
Disease: Generalized neonatal hypotonia
Generalized neonatal hypotonia 		20 0 1 5.0E-02 0 0
CUI: C1843885
Disease: Progressive gait ataxia
Progressive gait ataxia 		21 0 1 4.8E-02 0 0
CUI: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum 		21 0 1 4.8E-02 0 0
CUI: C0026961
Disease: Mydriasis
Mydriasis 		25 0 1 4.0E-02 0 0
CUI: C0282528
Disease: Peroxisomal Disorders
Peroxisomal Disorders 		25 0 1 4.0E-02 0 0
CUI: C0878638
Disease: Abnormality of the tongue
Abnormality of the tongue 		25 0 1 4.0E-02 0 0
CUI: C1837458
Disease: Impaired smooth pursuit
Impaired smooth pursuit 		25 0 1 4.0E-02 0 0
CUI: C3164407
Disease: Oligoasthenozoospermia
Oligoasthenozoospermia 		25 0 1 4.0E-02 0 0
CUI: C2749625
Disease: Motor axonal neuropathy
Motor axonal neuropathy 		27 0 1 3.7E-02 0 0
CUI: C1859126
Disease: Stippled epiphyses
Stippled epiphyses 		28 0 1 3.6E-02 0 0
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		36 0 1 2.8E-02 0 0