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: C4021805
Disease: Abnormality of the nasal bridge
Abnormality of the nasal bridge 		3 0 1 0.33 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: C0425782
Disease: Breast size
Breast size 		16 0 1 6.2E-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: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum 		21 0 1 4.8E-02 0 0
CUI: C3840083
Disease: Late closure of anterior fontanel
Late closure of anterior fontanel 		21 0 1 4.8E-02 0 0
CUI: C0041227
Disease: Trypanosomiasis
Trypanosomiasis 		23 0 1 4.3E-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: C0010093
Disease: Corpus Luteum Cyst
Corpus Luteum Cyst 		36 0 1 2.8E-02 0 0
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		36 0 1 2.8E-02 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology 		36 0 1 2.8E-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 0 1 2.4E-02 0 0
CUI: C0240421
Disease: Progressive muscle weakness
Progressive muscle weakness 		44 0 1 2.3E-02 0 0
CUI: C0546967
Disease: Posterior embryotoxon
Posterior embryotoxon 		44 0 1 2.3E-02 0 0
CUI: C1837402
Disease: Flat occiput
Flat occiput 		45 0 1 2.2E-02 0 0
CUI: C1842364
Disease: Central hypotonia
Central hypotonia 		50 0 1 2.0E-02 0 0
CUI: C1861869
Disease: Underdeveloped supraorbital ridges
Underdeveloped supraorbital ridges 		53 0 1 1.9E-02 0 0
CUI: C4316870
Disease: Abnormality of the eye
Abnormality of the eye 		56 0 1 1.8E-02 0 0