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: C2675021
Disease: Narrow palpebral fissure
Narrow palpebral fissure 		34 0 5 5.6E-02 0 0
CUI: C1456784
Disease: Paranoia
Paranoia 		35 0 5 5.6E-02 0 0
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius 		37 0 5 5.4E-02 0 0
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		611 0 34 5.3E-02 0 0
CUI: C1834055
Disease: Underdeveloped nasal alae
Underdeveloped nasal alae 		79 0 7 5.3E-02 0 0
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis 		106 0 8 5.1E-02 0 0
CUI: C0546967
Disease: Posterior embryotoxon
Posterior embryotoxon 		44 0 5 5.1E-02 0 0
CUI: C0345200
Disease: Congenital dysmotility of small intestine
Congenital dysmotility of small intestine 		3 0 3 5.0E-02 0 0
CUI: C1837084
Disease: Short metacarpal
Short metacarpal 		66 0 6 5.0E-02 0 0
CUI: C4022547
Disease: Elevated red cell adenosine deaminase activity
Elevated red cell adenosine deaminase activity 		3 0 3 5.0E-02 0 0
CUI: C4476616
Disease: Atrophic muscularis propria
Atrophic muscularis propria 		3 0 3 5.0E-02 0 0
CUI: C0740404
Disease: Limb defects
Limb defects 		67 0 6 5.0E-02 0 0
CUI: C0872218
Disease: MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME
MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME 		4 0 3 4.9E-02 0 0
CUI: C4024751
Disease: Abnormality of the extraocular muscles
Abnormality of the extraocular muscles 		4 0 3 4.9E-02 0 0
CUI: C0431890
Disease: Hypoplasia of thumb
Hypoplasia of thumb 		49 0 5 4.8E-02 0 0
CUI: C3277376
Disease: Multiple mitochondrial DNA deletions
Multiple mitochondrial DNA deletions 		6 0 3 4.8E-02 0 0
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		512 0 25 4.6E-02 0 0
CUI: C0432242
Disease: Desbuquois syndrome
Desbuquois syndrome 		9 0 3 4.5E-02 0 0
CUI: C1837256
Disease: Macrovesicular hepatic steatosis
Macrovesicular hepatic steatosis 		9 0 3 4.5E-02 0 0
CUI: C4023042
Disease: Abnormality of the mitochondrion
Abnormality of the mitochondrion 		10 0 3 4.5E-02 0 0
CUI: C0085577
Disease: Normocytic anemia
Normocytic anemia 		12 0 3 4.3E-02 0 0
CUI: C0086795
Disease: Pfaundler-Hurler Syndrome
Pfaundler-Hurler Syndrome 		36 0 4 4.3E-02 0 0
CUI: C4476793
Disease: Abnormal cell morphology
Abnormal cell morphology 		12 0 3 4.3E-02 0 0
CUI: C0266013
Disease: Congenital hypoplasia of breast
Congenital hypoplasia of breast 		38 0 4 4.3E-02 0 0
CUI: C0545053
Disease: Advanced bone age
Advanced bone age 		64 0 5 4.2E-02 0 0