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: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
145 0 1 3.7E-03 0 0
CUI: C1136382
Disease: Sclerocystic Ovaries
Sclerocystic Ovaries
144 0 1 3.8E-03 0 0
CUI: C0014518
Disease: Toxic Epidermal Necrolysis
Toxic Epidermal Necrolysis
143 0 1 3.8E-03 0 0
CUI: C1868571
Disease: Highly arched eyebrow
Highly arched eyebrow
141 0 1 3.8E-03 0 0
CUI: C0026640
Disease: Mouth Neoplasms
Mouth Neoplasms
140 0 1 3.8E-03 0 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition
140 0 1 3.8E-03 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
139 0 1 3.8E-03 0 0
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
139 0 1 3.8E-03 0 0
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
139 0 1 3.8E-03 0 0
CUI: C0005938
Disease: Bone Density
Bone Density
138 0 1 3.8E-03 0 0
CUI: C1963094
Disease: Dry Skin, CTCAE
Dry Skin, CTCAE
137 0 1 3.9E-03 0 0
CUI: C0022602
Disease: Actinic keratosis
Actinic keratosis
136 0 1 3.9E-03 0 0
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
135 0 1 3.9E-03 0 0
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome
130 0 1 4.0E-03 0 0
CUI: C0079924
Disease: Oligohydramnios
Oligohydramnios
129 0 1 4.0E-03 0 0
CUI: C0241355
Disease: Small testicle
Small testicle
129 0 1 4.0E-03 0 0
CUI: C1837404
Disease: High, narrow palate
High, narrow palate
129 0 1 4.0E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria
127 0 1 4.0E-03 0 0
CUI: C0019208
Disease: Hepatoma, Novikoff
Hepatoma, Novikoff
125 0 1 4.0E-03 0 0
CUI: C0019207
Disease: Hepatoma, Morris
Hepatoma, Morris
124 0 1 4.1E-03 0 0
Creatinine measurement, serum (procedure)
124 0 1 4.1E-03 0 0
CUI: C3805574
Disease: Increased fracture rate
Increased fracture rate
123 0 1 4.1E-03 0 0
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
611 0 3 4.1E-03 0 0
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies
121 0 1 4.1E-03 0 0
CUI: C1856689
Disease: FRIEDREICH ATAXIA 1
FRIEDREICH ATAXIA 1
119 0 1 4.1E-03 0 0