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: C1848201
Disease: Subcortical Band Heterotopia
Subcortical Band Heterotopia 		30 0 10 0.15 0 0
CUI: C0266463
Disease: Lissencephaly
Lissencephaly 		71 0 10 9.4E-02 0 0
CUI: C0241654
Disease: Abnormal heart valve morphology
Abnormal heart valve morphology 		42 0 7 8.7E-02 0 0
CUI: C1281373
Disease: Intercritical gout
Intercritical gout 		6 0 4 8.5E-02 0 0
CUI: C4551969
Disease: Bilateral Periventricular Nodular Heterotopia
Bilateral Periventricular Nodular Heterotopia 		6 0 4 8.5E-02 0 0
CUI: C0521175
Disease: Neuropil Threads
Neuropil Threads 		13 0 4 7.4E-02 0 0
CUI: C1458140
Disease: Bleeding tendency
Bleeding tendency 		71 0 8 7.4E-02 0 0
CUI: C1801950
Disease: Opitz-G syndrome, type 2
Opitz-G syndrome, type 2 		13 0 4 7.4E-02 0 0
CUI: C1848199
Disease: X-Linked Lissencephaly
X-Linked Lissencephaly 		14 0 4 7.3E-02 0 0
CUI: C0266449
Disease: Congenital anomaly of brain
Congenital anomaly of brain 		103 0 10 7.2E-02 0 0
CUI: C1321546
Disease: Anaplastic large B-cell lymphoma
Anaplastic large B-cell lymphoma 		17 0 4 6.9E-02 0 0
CUI: C0266491
Disease: Neuronal heterotopia
Neuronal heterotopia 		67 0 7 6.7E-02 0 0
CUI: C0393570
Disease: Corticobasal degeneration
Corticobasal degeneration 		35 0 5 6.7E-02 0 0
CUI: C1842563
Disease: Heterotopia, Periventricular, Autosomal Recessive
Heterotopia, Periventricular, Autosomal Recessive 		3 0 3 6.7E-02 0 0
CUI: C1848213
Disease: Periventricular Heterotopia, X-Linked
Periventricular Heterotopia, X-Linked 		3 38 3 6.7E-02 5 8.1E-02
CUI: C0034194
Disease: Pyloric Stenosis
Pyloric Stenosis 		121 0 10 6.4E-02 0 0
CUI: C0423757
Disease: Thin skin
Thin skin 		77 0 7 6.1E-02 0 0
CUI: C0456132
Disease: Large fontanelle
Large fontanelle 		77 0 7 6.1E-02 0 0
CUI: C0431380
Disease: Cortical Dysplasia
Cortical Dysplasia 		118 0 9 5.8E-02 0 0
CUI: C4024202
Disease: Reduced number of teeth
Reduced number of teeth 		67 0 6 5.7E-02 0 0
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia 		226 0 14 5.4E-02 0 0
CUI: C0266568
Disease: Persistent Hyperplastic Primary Vitreous
Persistent Hyperplastic Primary Vitreous 		33 0 4 5.4E-02 0 0
CUI: C1840309
Disease: Short 4th metacarpal
Short 4th metacarpal 		14 0 3 5.4E-02 0 0
CUI: C1838705
Disease: Anteriorly placed anus
Anteriorly placed anus 		34 0 4 5.3E-02 0 0
CUI: C0041228
Disease: African Trypanosomiasis
African Trypanosomiasis 		55 0 5 5.3E-02 0 0