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: C0410935
Disease: Wide cranial sutures
Wide cranial sutures 		10 0 3 9.4E-02 0 0
CUI: C2931356
Disease: Spastic paraplegia type 5A, recessive
Spastic paraplegia type 5A, recessive 		13 0 3 8.6E-02 0 0
CUI: C0268354
Disease: De Barsy syndrome
De Barsy syndrome 		2 0 2 8.0E-02 0 0
CUI: C2751987
Disease: Cutis Laxa, Autosomal Recessive, Type IIB
Cutis Laxa, Autosomal Recessive, Type IIB 		2 0 2 8.0E-02 0 0
CUI: C4022871
Disease: Extra-axial cerebrospinal fluid accumulation
Extra-axial cerebrospinal fluid accumulation 		2 1 2 8.0E-02 1 0.33
CUI: C0008519
Disease: Ectopic Tissue
Ectopic Tissue 		3 4 2 7.7E-02 1 0.17
CUI: C1842563
Disease: Heterotopia, Periventricular, Autosomal Recessive
Heterotopia, Periventricular, Autosomal Recessive 		3 0 2 7.7E-02 0 0
CUI: C1849128
Disease: Spastic paraplegia 15, autosomal recessive
Spastic paraplegia 15, autosomal recessive 		3 0 2 7.7E-02 0 0
CUI: C4021884
Disease: Bilateral choanal atresia/stenosis
Bilateral choanal atresia/stenosis 		3 0 2 7.7E-02 0 0
CUI: C1832390
Disease: Van Maldergem Wetzburger Verloes syndrome
Van Maldergem Wetzburger Verloes syndrome 		4 0 2 7.4E-02 0 0
CUI: C1849173
Disease: Periventricular gray matter heterotopia
Periventricular gray matter heterotopia 		4 0 2 7.4E-02 0 0
CUI: C0266304
Disease: Double kidney (disorder)
Double kidney (disorder) 		6 0 2 6.9E-02 0 0
CUI: C1844508
Disease: Large foramen magnum
Large foramen magnum 		6 0 2 6.9E-02 0 0
CUI: C1856765
Disease: Irregular dentition
Irregular dentition 		6 0 2 6.9E-02 0 0
CUI: C3277117
Disease: Caudal appendage
Caudal appendage 		6 0 2 6.9E-02 0 0
CUI: C4023342
Disease: Gastrostomy tube feeding in infancy
Gastrostomy tube feeding in infancy 		38 0 4 6.8E-02 0 0
CUI: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4 		7 0 2 6.7E-02 0 0
CUI: C1848514
Disease: Short fourth metatarsal
Short fourth metatarsal 		8 0 2 6.5E-02 0 0
CUI: C4021217
Disease: EEG with generalized slow activity
EEG with generalized slow activity 		8 6 2 6.5E-02 1 0.12
CUI: C4022739
Disease: Abnormal neuron morphology
Abnormal neuron morphology 		8 0 2 6.5E-02 0 0
CUI: C0563243
Disease: Poor coordination
Poor coordination 		26 8 3 6.2E-02 2 0.22
CUI: C0796147
Disease: Acrocallosal Syndrome
Acrocallosal Syndrome 		9 0 2 6.2E-02 0 0
CUI: C1854372
Disease: Impaired vibration sensation at ankles
Impaired vibration sensation at ankles 		9 0 2 6.2E-02 0 0
CUI: C1955869
Disease: Malformations of Cortical Development
Malformations of Cortical Development 		60 0 5 6.2E-02 0 0
CUI: C2677504
Disease: AUTISM, SUSCEPTIBILITY TO, 15
AUTISM, SUSCEPTIBILITY TO, 15 		9 0 2 6.2E-02 0 0