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: C3151187
Disease: SECKEL SYNDROME 5
SECKEL SYNDROME 5 		2 0 2 6.1E-02 0 0
CUI: C3809431
Disease: MICROCEPHALY 11, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 11, PRIMARY, AUTOSOMAL RECESSIVE 		2 0 2 6.1E-02 0 0
CUI: C0265205
Disease: Robinow Syndrome
Robinow Syndrome 		20 0 3 6.0E-02 0 0
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly 		410 0 25 6.0E-02 0 0
CUI: C1857656
Disease: Prematurely aged appearance
Prematurely aged appearance 		40 0 4 5.8E-02 0 0
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		427 0 25 5.7E-02 0 0
CUI: C4274995
Disease: Lissencephaly with cerebellar hypoplasia
Lissencephaly with cerebellar hypoplasia 		4 0 2 5.7E-02 0 0
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		429 0 24 5.5E-02 0 0
CUI: C1563697
Disease: Chromosome Instability Syndromes
Chromosome Instability Syndromes 		6 0 2 5.4E-02 0 0
CUI: C4024202
Disease: Reduced number of teeth
Reduced number of teeth 		67 0 5 5.3E-02 0 0
CUI: C1865037
Disease: Cone-shaped epiphysis
Cone-shaped epiphysis 		49 0 4 5.1E-02 0 0
CUI: C1970308
Disease: Selective tooth agenesis
Selective tooth agenesis 		8 0 2 5.1E-02 0 0
CUI: C0342185
Disease: Hyperthyroxinemia, Familial Dysalbuminemic
Hyperthyroxinemia, Familial Dysalbuminemic 		12 0 2 4.7E-02 0 0
CUI: C3853041
Disease: Severe Congenital Microcephaly
Severe Congenital Microcephaly 		35 0 3 4.6E-02 0 0
CUI: C0393754
Disease: Headache associated with sexual activity
Headache associated with sexual activity 		14 0 2 4.4E-02 0 0
CUI: C1840069
Disease: Sandal gap
Sandal gap 		62 0 4 4.4E-02 0 0
CUI: C0456065
Disease: Infant, Extremely Low Birth Weight
Infant, Extremely Low Birth Weight 		15 0 2 4.3E-02 0 0
CUI: C1837463
Disease: Narrow face
Narrow face 		87 0 5 4.3E-02 0 0
CUI: C3494623
Disease: Mild dementia
Mild dementia 		16 0 2 4.3E-02 0 0
CUI: C0153943
Disease: Benign neoplasm of stomach
Benign neoplasm of stomach 		17 0 2 4.2E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome 		42 0 3 4.2E-02 0 0
CUI: C0496905
Disease: Neoplasm of uncertain or unknown behavior of stomach
Neoplasm of uncertain or unknown behavior of stomach 		17 0 2 4.2E-02 0 0
CUI: C0033246
Disease: Proctitis
Proctitis 		18 0 2 4.1E-02 0 0
CUI: C0240538
Disease: Convex nasal ridge
Convex nasal ridge 		69 0 4 4.1E-02 0 0
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum 		615 0 25 4.0E-02 0 0