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: C0241355
Disease: Small testicle
Small testicle
129 0 1 2.2E-03 0 0
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet
129 0 1 2.2E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary
123 0 1 2.2E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia
121 0 1 2.2E-03 0 0
CUI: C0025521
Disease: Inborn Errors of Metabolism
Inborn Errors of Metabolism
119 0 1 2.2E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography
119 0 1 2.2E-03 0 0
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia
118 0 1 2.2E-03 0 0
CUI: C0576226
Disease: Short foot
Short foot
116 0 1 2.2E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination
112 0 1 2.2E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities
112 0 1 2.2E-03 0 0
CUI: C0431447
Disease: Synophrys
Synophrys
111 0 1 2.2E-03 0 0
CUI: C0424574
Disease: Duration of sleep
Duration of sleep
104 0 1 2.3E-03 0 0
CUI: C1853487
Disease: Thick eyebrow
Thick eyebrow
104 0 1 2.3E-03 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin
101 0 1 2.3E-03 0 0
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc
98 0 1 2.3E-03 0 0
CUI: C0850703
Disease: Frequent falls
Frequent falls
94 0 1 2.3E-03 0 0
CUI: C0566620
Disease: Nasal voice
Nasal voice
93 0 1 2.3E-03 0 0
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
90 0 1 2.4E-03 0 0
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution
90 0 1 2.4E-03 0 0
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
89 0 1 2.4E-03 0 0
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
89 0 1 2.4E-03 0 0
Respiratory insufficiency due to muscle weakness
85 0 1 2.4E-03 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 2.4E-03 0 0
CUI: C1853241
Disease: Flat face
Flat face
83 0 1 2.4E-03 0 0
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen
80 0 1 2.4E-03 0 0