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: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
249 0 1 1.8E-03 0 0
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos
235 0 1 1.9E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 1 2.1E-03 0 0
Child Development Disorders, Pervasive
168 0 1 2.1E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 2.2E-03 0 0
CUI: C0221358
Disease: Long narrow head
Long narrow head
154 0 1 2.2E-03 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism
148 0 1 2.2E-03 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion
145 0 1 2.3E-03 0 0
CUI: C0152423
Disease: Congenital small ears
Congenital small ears
137 0 1 2.3E-03 0 0
CUI: C1849089
Disease: Broad forehead
Broad forehead
133 0 1 2.3E-03 0 0
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet
129 0 1 2.3E-03 0 0
CUI: C0039075
Disease: Syndactyly
Syndactyly
127 0 1 2.3E-03 0 0
CUI: C0426429
Disease: Broad nasal tip
Broad nasal tip
125 0 1 2.4E-03 0 0
CUI: C0240543
Disease: Bulbous nose
Bulbous nose
123 0 1 2.4E-03 0 0
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia
118 0 1 2.4E-03 0 0
CUI: C0576226
Disease: Short foot
Short foot
116 0 1 2.4E-03 0 0
Aplasia/Hypoplasia of the cerebellum
116 0 1 2.4E-03 0 0
CUI: C0024421
Disease: Macroglossia
Macroglossia
115 0 1 2.4E-03 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity
113 0 1 2.4E-03 0 0
CUI: C0426790
Disease: Narrow thorax
Narrow thorax
112 0 1 2.4E-03 0 0
CUI: C1837770
Disease: Sparse hair
Sparse hair
112 0 1 2.4E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities
112 0 1 2.4E-03 0 0
CUI: C1853237
Disease: Isolated cases
Isolated cases
111 0 1 2.4E-03 0 0
CUI: C1843108
Disease: Short palm
Short palm
110 0 1 2.4E-03 0 0
CUI: C0575802
Disease: Small hand
Small hand
108 0 1 2.5E-03 0 0