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: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
251 0 1 2.0E-03 0 0
CUI: C3888194
Disease: MIXED LINEAGE LEUKEMIA
MIXED LINEAGE LEUKEMIA
240 0 1 2.1E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 2 2.5E-03 0 0
CUI: C4025790
Disease: Specific learning disability
Specific learning disability
165 0 1 2.5E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation
160 0 1 2.5E-03 0 0
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
149 0 1 2.6E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency
148 0 1 2.6E-03 0 0
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
147 0 1 2.6E-03 0 0
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
147 0 1 2.6E-03 0 0
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
147 0 1 2.6E-03 0 0
CUI: C1851584
Disease: Childhood Ependymoma
Childhood Ependymoma
147 0 1 2.6E-03 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia
144 0 1 2.6E-03 0 0
CUI: C0278874
Disease: Adult Ependymoma
Adult Ependymoma
144 0 1 2.6E-03 0 0
Newly Diagnosed Childhood Ependymoma
144 0 1 2.6E-03 0 0
CUI: C0025363
Disease: Mental Retardation, Psychosocial
Mental Retardation, Psychosocial
142 0 1 2.6E-03 0 0
CUI: C1868571
Disease: Highly arched eyebrow
Highly arched eyebrow
141 0 1 2.6E-03 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
139 0 1 2.7E-03 0 0
CUI: C1998028
Disease: Photoreceptor degeneration
Photoreceptor degeneration
136 0 1 2.7E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color
130 0 1 2.7E-03 0 0
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet
129 0 1 2.7E-03 0 0
CUI: C0039075
Disease: Syndactyly
Syndactyly
127 0 1 2.7E-03 0 0
CUI: C0240543
Disease: Bulbous nose
Bulbous nose
123 0 1 2.8E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography
119 0 1 2.8E-03 0 0
Childhood T Acute Lymphoblastic Leukemia
119 0 1 2.8E-03 0 0
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay
118 0 1 2.8E-03 0 0