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: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
291 0 1 2.2E-03 0 0
CUI: C0521525
Disease: Short neck
Short neck
288 0 1 2.2E-03 0 0
CUI: C0489786
Disease: Height
Height
249 0 1 2.4E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
237 0 1 2.5E-03 0 0
Platelet mean volume determination (procedure)
223 0 1 2.6E-03 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis
217 0 1 2.6E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia
216 0 1 2.6E-03 0 0
CUI: C1843367
Disease: Poor school performance
Poor school performance
211 0 1 2.6E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
208 0 1 2.7E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 2.7E-03 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia
191 0 1 2.8E-03 0 0
Small for gestational age (disorder)
181 0 1 2.9E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge
180 0 1 2.9E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability
854 0 3 2.9E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia
169 0 1 3.0E-03 0 0
Child Development Disorders, Pervasive
168 0 1 3.0E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 3.0E-03 0 0
CUI: C4025790
Disease: Specific learning disability
Specific learning disability
165 0 1 3.0E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation
160 0 1 3.0E-03 0 0
CUI: C0023380
Disease: Lethargy
Lethargy
160 0 1 3.0E-03 0 0
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers
160 0 1 3.0E-03 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead
149 0 1 3.2E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency
148 0 1 3.2E-03 0 0
CUI: C4551485
Disease: Clinodactyly
Clinodactyly
148 0 1 3.2E-03 0 0
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
147 0 1 3.2E-03 0 0