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: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal 		130 0 1 4.1E-03 0 0
CUI: C0241355
Disease: Small testicle
Small testicle 		129 0 1 4.1E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria 		129 0 1 4.1E-03 0 0
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet 		129 0 1 4.1E-03 0 0
CUI: C0236969
Disease: Substance-Related Disorders
Substance-Related Disorders 		128 0 1 4.1E-03 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision 		127 0 1 4.1E-03 0 0
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		122 0 1 4.2E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		121 0 1 4.2E-03 0 0
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle 		118 0 1 4.3E-03 0 0
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia 		118 0 1 4.3E-03 0 0
CUI: C0576226
Disease: Short foot
Short foot 		116 0 1 4.3E-03 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision 		115 0 1 4.3E-03 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 1 4.3E-03 0 0
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 3 4.3E-03 0 0
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness 		112 0 1 4.4E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		112 0 1 4.4E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities 		112 0 1 4.4E-03 0 0
CUI: C0431447
Disease: Synophrys
Synophrys 		111 0 1 4.4E-03 0 0
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		110 0 1 4.4E-03 0 0
CUI: C0085631
Disease: Agitation
Agitation 		109 0 1 4.4E-03 0 0
CUI: C0266362
Disease: Ambiguous Genitalia
Ambiguous Genitalia 		109 0 1 4.4E-03 0 0
CUI: C0575802
Disease: Small hand
Small hand 		108 0 1 4.5E-03 0 0
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 1 4.5E-03 0 0
CUI: C0342276
Disease: Maturity onset diabetes mellitus in young
Maturity onset diabetes mellitus in young 		105 0 1 4.5E-03 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures 		105 0 1 4.5E-03 0 0