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: C3553950
Disease: PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 8
PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 8 		1 0 1 1.00 0 0
CUI: C3553951
Disease: PEROXISOME BIOGENESIS DISORDER 7B
PEROXISOME BIOGENESIS DISORDER 7B 		1 5 1 1.00 4 0.50
CUI: C2750798
Disease: Polymicrogyria With Optic Nerve Hypoplasia
Polymicrogyria With Optic Nerve Hypoplasia 		2 0 1 0.50 0 0
CUI: C1856186
Disease: Deafness enamel hypoplasia nail defects
Deafness enamel hypoplasia nail defects 		3 0 1 0.33 0 0
CUI: C3550234
Disease: PEROXISOME BIOGENESIS DISORDER 2B
PEROXISOME BIOGENESIS DISORDER 2B 		5 0 1 0.20 0 0
CUI: C3550693
Disease: PEROXISOME BIOGENESIS DISORDER 3B
PEROXISOME BIOGENESIS DISORDER 3B 		5 0 1 0.20 0 0
CUI: C0677600
Disease: Inspiratory stridor
Inspiratory stridor 		8 2 1 0.12 1 0.12
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: C1840319
Disease: Redundant neck skin
Redundant neck skin 		16 3 1 6.2E-02 1 0.11
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: C1845123
Disease: Generalized neonatal hypotonia
Generalized neonatal hypotonia 		20 0 1 5.0E-02 0 0
CUI: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum 		21 0 1 4.8E-02 0 0
CUI: C0878638
Disease: Abnormality of the tongue
Abnormality of the tongue 		25 0 1 4.0E-02 0 0
CUI: C1859126
Disease: Stippled epiphyses
Stippled epiphyses 		28 0 1 3.6E-02 0 0
CUI: C3539168
Disease: PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A
PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A 		34 3 1 2.9E-02 2 0.25
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		36 1 1 2.8E-02 1 0.14
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology 		36 0 1 2.8E-02 0 0
CUI: C1527231
Disease: Adrenomyeloneuropathy
Adrenomyeloneuropathy 		38 0 1 2.6E-02 0 0
CUI: C4021815
Disease: Abnormal palate morphology
Abnormal palate morphology 		40 0 1 2.5E-02 0 0
CUI: C1832200
Disease: Peroxisome biogenesis disorders
Peroxisome biogenesis disorders 		41 38 1 2.4E-02 2 4.7E-02