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: C0029928
Disease: Ovarian Diseases
Ovarian Diseases
0 5 0 0 1 8.0E-04
CUI: C0033923
Disease: Psychomotor Performance
Psychomotor Performance
0 1 0 0 1 8.0E-04
CUI: C0523550
Disease: Catalase measurement
Catalase measurement
0 2 0 0 1 8.0E-04
CUI: C0678189
Disease: Hyperlipidemia, group A
Hyperlipidemia, group A
0 1 0 0 1 8.0E-04
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous
0 2 0 0 1 8.0E-04
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis
0 2 0 0 1 8.0E-04
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
0 1 0 0 1 8.0E-04
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 10
0 1 0 0 1 8.0E-04
CUI: C3899405
Disease: Decreased Attention
Decreased Attention
0 3 0 0 1 8.0E-04
CUI: C1854882
Disease: Absent speech
Absent speech
232 0 1 1.4E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 1 1.5E-03 0 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive
172 0 1 1.5E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control
162 0 1 1.5E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady
143 0 1 1.6E-03 0 0
CUI: C1868571
Disease: Highly arched eyebrow
Highly arched eyebrow
141 0 1 1.6E-03 0 0
CUI: C4024896
Disease: Motor neuron atrophy
Motor neuron atrophy
138 0 1 1.6E-03 0 0
CUI: C0240310
Disease: Hypoplasia of the maxilla
Hypoplasia of the maxilla
113 0 1 1.7E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination
112 0 1 1.7E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities
112 0 1 1.7E-03 0 0
CUI: C1843108
Disease: Short palm
Short palm
110 0 1 1.7E-03 0 0
CUI: C0023479
Disease: Acute myelomonocytic leukemia
Acute myelomonocytic leukemia
105 0 1 1.7E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis
104 0 1 1.7E-03 0 0
CUI: C1837142
Disease: Poor suck
Poor suck
103 0 1 1.7E-03 0 0
Splenic Marginal Zone B-Cell Lymphoma
93 0 1 1.7E-03 0 0
CUI: C0398686
Disease: Primary immune deficiency disorder
Primary immune deficiency disorder
93 0 1 1.7E-03 0 0