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: C4054546
Disease: Melanocortin 4 Receptor Deficiency
Melanocortin 4 Receptor Deficiency 		24 0 1 4.4E-04 0 0
CUI: C0155707
Disease: Trifascicular block
Trifascicular block 		23 0 1 4.4E-04 0 0
CUI: C1849923
Disease: Generalized hypopigmentation
Generalized hypopigmentation 		23 0 1 4.4E-04 0 0
CUI: C4023683
Disease: EEG with spike-wave complexes
EEG with spike-wave complexes 		23 0 1 4.4E-04 0 0
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		22 0 1 4.4E-04 0 0
CUI: C0265213
Disease: Distal arthrogryposis syndrome
Distal arthrogryposis syndrome 		22 0 1 4.4E-04 0 0
CUI: C1866012
Disease: Proximal muscle weakness in upper limbs
Proximal muscle weakness in upper limbs 		22 0 1 4.4E-04 0 0
CUI: C1838114
Disease: Generalized limb muscle atrophy
Generalized limb muscle atrophy 		21 0 1 4.4E-04 0 0
CUI: C1856660
Disease: Abnormality of the helix
Abnormality of the helix 		21 0 1 4.4E-04 0 0
CUI: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum 		21 0 1 4.4E-04 0 0
CUI: C4024809
Disease: Chorioretinal dysplasia
Chorioretinal dysplasia 		21 0 1 4.4E-04 0 0
CUI: C0006852
Disease: Candidiasis of vagina
Candidiasis of vagina 		20 0 1 4.4E-04 0 0
CUI: C0241700
Disease: Voice Fatigue
Voice Fatigue 		20 0 1 4.4E-04 0 0
CUI: C1963175
Disease: Sinus Bradycardia, CTCAE
Sinus Bradycardia, CTCAE 		20 0 1 4.4E-04 0 0
CUI: C2108107
Disease: continuous electrocardiogram sinus bradycardia (finding)
continuous electrocardiogram sinus bradycardia (finding) 		20 0 1 4.4E-04 0 0
CUI: C2936862
Disease: Bardet-Biedl syndrome 1 (disorder)
Bardet-Biedl syndrome 1 (disorder) 		20 0 1 4.4E-04 0 0
CUI: C3696376
Disease: 3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria 		20 0 1 4.4E-04 0 0
CUI: C0029294
Disease: Orofaciodigital Syndromes
Orofaciodigital Syndromes 		19 0 1 4.4E-04 0 0
CUI: C0272278
Disease: Congenital thrombocytopenia
Congenital thrombocytopenia 		19 0 1 4.4E-04 0 0
CUI: C0334013
Disease: Phrynoderma
Phrynoderma 		19 0 1 4.4E-04 0 0
CUI: C0343073
Disease: Wooly hair
Wooly hair 		19 0 1 4.4E-04 0 0
CUI: C0457133
Disease: Muscle eye brain disease
Muscle eye brain disease 		19 0 1 4.4E-04 0 0
CUI: C1846435
Disease: Disproportionate short-trunk short stature
Disproportionate short-trunk short stature 		19 0 1 4.4E-04 0 0
CUI: C1969156
Disease: EEG with burst suppression
EEG with burst suppression 		19 0 1 4.4E-04 0 0
CUI: C4024921
Disease: Lower limb amyotrophy
Lower limb amyotrophy 		19 0 1 4.4E-04 0 0