Source: ALL
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: C0278061
Disease: Abnormal mental state
Abnormal mental state 		24 0 17 0.52 0 0
CUI: C0683322
Disease: Mental impairment
Mental impairment 		67 0 16 0.21 0 0
CUI: C3825158
Disease: Learning disabled
Learning disabled 		3 0 3 0.12 0 0
CUI: C0004444
Disease: Avoidant Personality Disorder
Avoidant Personality Disorder 		4 0 3 0.11 0 0
CUI: C0751156
Disease: FRAXA Syndrome
FRAXA Syndrome 		8 0 3 9.7E-02 0 0
CUI: C0031572
Disease: Phobia, Social
Phobia, Social 		33 0 5 9.3E-02 0 0
CUI: C2748208
Disease: Executive dysfunction
Executive dysfunction 		33 0 5 9.3E-02 0 0
CUI: C1864172
Disease: Peroxisome Biogenesis Disorder, Complementation Group G
Peroxisome Biogenesis Disorder, Complementation Group G 		10 0 3 9.1E-02 0 0
CUI: C0751157
Disease: FRAXE Syndrome
FRAXE Syndrome 		11 0 3 8.8E-02 0 0
CUI: C1656427
Disease: Early onset schizophrenia
Early onset schizophrenia 		15 0 3 7.9E-02 0 0
CUI: C1260405
Disease: frontal dementia
frontal dementia 		2 0 2 7.7E-02 0 0
CUI: C0262405
Disease: Cerebral dysfunction
Cerebral dysfunction 		45 0 5 7.6E-02 0 0
CUI: C2930861
Disease: Premature ovarian failure, familial
Premature ovarian failure, familial 		3 0 2 7.4E-02 0 0
CUI: C4024589
Disease: Aplasia/Hypoplasia of the mandible
Aplasia/Hypoplasia of the mandible 		19 0 3 7.1E-02 0 0
CUI: C3277753
Disease: Deep-set nails
Deep-set nails 		5 0 2 6.9E-02 0 0
CUI: C0012746
Disease: Dissociative disorder
Dissociative disorder 		6 0 2 6.7E-02 0 0
CUI: C0520823
Disease: Patellar clonus
Patellar clonus 		6 0 2 6.7E-02 0 0
CUI: C4552213
Disease: Broad autism phenotype
Broad autism phenotype 		6 0 2 6.7E-02 0 0
CUI: C0231796
Disease: respiratory abnormalities
respiratory abnormalities 		7 0 2 6.5E-02 0 0
CUI: C4054546
Disease: Melanocortin 4 Receptor Deficiency
Melanocortin 4 Receptor Deficiency 		24 0 3 6.4E-02 0 0
CUI: C4023014
Disease: Stereotypical hand wringing
Stereotypical hand wringing 		8 0 2 6.2E-02 0 0
CUI: C0265339
Disease: Borjeson-Forssman-Lehmann syndrome
Borjeson-Forssman-Lehmann syndrome 		9 0 2 6.1E-02 0 0
CUI: C0338657
Disease: Age-associated memory impairment
Age-associated memory impairment 		9 0 2 6.1E-02 0 0
CUI: C4019039
Disease: Intestinal obstruction co-occurrent and due to decreased peristalsis
Intestinal obstruction co-occurrent and due to decreased peristalsis 		9 0 2 6.1E-02 0 0
CUI: C2931498
Disease: Mental Retardation, X-Linked 1
Mental Retardation, X-Linked 1 		45 0 4 6.0E-02 0 0