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: C0016242
Disease: Vitreous floaters
Vitreous floaters 		4 0 1 0.12 0 0
CUI: C4020922
Disease: Enlarged fossa interpeduncularis
Enlarged fossa interpeduncularis 		4 0 1 0.12 0 0
CUI: C4024941
Disease: Dilated third ventricle
Dilated third ventricle 		4 0 1 0.12 0 0
CUI: C4025719
Disease: Dysgenesis of the cerebellar vermis
Dysgenesis of the cerebellar vermis 		4 0 1 0.12 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI 		35 0 4 0.11 0 0
CUI: C3472600
Disease: Chronic hepatitis E
Chronic hepatitis E 		5 0 1 0.11 0 0
CUI: C3806216
Disease: Neonatal breathing dysregulation
Neonatal breathing dysregulation 		5 0 1 0.11 0 0
CUI: C4274118
Disease: Joubert syndrome with ocular defect
Joubert syndrome with ocular defect 		5 0 1 0.11 0 0
CUI: C1844925
Disease: Cervical spinal canal stenosis
Cervical spinal canal stenosis 		6 0 1 1.0E-01 0 0
CUI: C4021606
Disease: Mesoaxial hand polydactyly
Mesoaxial hand polydactyly 		6 0 1 1.0E-01 0 0
CUI: C0175692
Disease: Johanson-Blizzard syndrome
Johanson-Blizzard syndrome 		7 0 1 9.1E-02 0 0
CUI: C1836320
Disease: Proximal femoral metaphyseal irregularity
Proximal femoral metaphyseal irregularity 		7 0 1 9.1E-02 0 0
CUI: C1969532
Disease: Rhizomelic arm shortening
Rhizomelic arm shortening 		7 0 1 9.1E-02 0 0
CUI: C4021739
Disease: Abnormality of the acetabulum
Abnormality of the acetabulum 		7 0 1 9.1E-02 0 0
CUI: C1851853
Disease: Midline notch of upper alveolar ridge
Midline notch of upper alveolar ridge 		8 0 1 8.3E-02 0 0
CUI: C1854418
Disease: Biparietal narrowing
Biparietal narrowing 		60 0 5 8.3E-02 0 0
CUI: C4020690
Disease: Abnormality of peripheral nerve conduction
Abnormality of peripheral nerve conduction 		8 0 1 8.3E-02 0 0
CUI: C4021581
Disease: Distal upper limb amyotrophy
Distal upper limb amyotrophy 		8 0 1 8.3E-02 0 0
CUI: C4024597
Disease: Aplasia/Hypoplasia involving the pelvis
Aplasia/Hypoplasia involving the pelvis 		8 0 1 8.3E-02 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes 		61 0 5 8.2E-02 0 0
CUI: C1848595
Disease: Mesoaxial polydactyly
Mesoaxial polydactyly 		9 0 1 7.7E-02 0 0
CUI: C1848597
Disease: Central Y-shaped metacarpal
Central Y-shaped metacarpal 		9 0 1 7.7E-02 0 0
CUI: C1856655
Disease: Hypoplasia of olfactory tract
Hypoplasia of olfactory tract 		9 0 1 7.7E-02 0 0
CUI: C2681923
Disease: RETINITIS PIGMENTOSA 2 (disorder)
RETINITIS PIGMENTOSA 2 (disorder) 		9 0 1 7.7E-02 0 0
CUI: C0426808
Disease: Long clavicle
Long clavicle 		10 0 1 7.1E-02 0 0