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: C0008412
Disease: Choline Deficiency
Choline Deficiency 		16 0 1 3.7E-02 0 0
CUI: C1858712
Disease: Spastic paraplegia 10, autosomal dominant
Spastic paraplegia 10, autosomal dominant 		16 0 1 3.7E-02 0 0
CUI: C0009373
Disease: Colonic Diseases
Colonic Diseases 		17 0 1 3.6E-02 0 0
CUI: C0699739
Disease: Sensory Neuropathy, Hereditary
Sensory Neuropathy, Hereditary 		19 0 1 3.3E-02 0 0
CUI: C1845245
Disease: Lower limb hypertonia
Lower limb hypertonia 		21 0 1 3.1E-02 0 0
CUI: C1846566
Disease: Degeneration of the lateral corticospinal tracts
Degeneration of the lateral corticospinal tracts 		21 0 1 3.1E-02 0 0
CUI: C0027889
Disease: Hereditary Sensory and Autonomic Neuropathies
Hereditary Sensory and Autonomic Neuropathies 		25 0 1 2.8E-02 0 0
CUI: C0201544
Disease: Prostate specific antigen measurement
Prostate specific antigen measurement 		25 0 1 2.8E-02 0 0
CUI: C0221163
Disease: Motor Disorders
Motor Disorders 		25 0 1 2.8E-02 0 0
CUI: C0002888
Disease: Anemia, Megaloblastic
Anemia, Megaloblastic 		26 0 1 2.7E-02 0 0
CUI: C1863416
Disease: Autosomal dominant compelling helio ophthalmic outburst syndrome
Autosomal dominant compelling helio ophthalmic outburst syndrome 		26 0 1 2.7E-02 0 0
CUI: C0751602
Disease: Hereditary Autosomal Dominant Spastic Paraplegia
Hereditary Autosomal Dominant Spastic Paraplegia 		27 0 1 2.6E-02 0 0
CUI: C0011999
Disease: Diastematomyelia
Diastematomyelia 		28 0 1 2.6E-02 0 0
CUI: C0152234
Disease: Iniencephaly
Iniencephaly 		28 0 1 2.6E-02 0 0
CUI: C0344479
Disease: Spinal Cord Myelodysplasia
Spinal Cord Myelodysplasia 		28 0 1 2.6E-02 0 0
CUI: C1843663
Disease: Urinary bladder sphincter dysfunction
Urinary bladder sphincter dysfunction 		28 0 1 2.6E-02 0 0
CUI: C0027806
Disease: Neurenteric Cyst
Neurenteric Cyst 		29 0 1 2.5E-02 0 0
CUI: C1836451
Disease: Distal lower limb amyotrophy
Distal lower limb amyotrophy 		29 0 1 2.5E-02 0 0
CUI: C0702169
Disease: Acrania
Acrania 		31 0 1 2.4E-02 0 0
CUI: C0020071
Disease: Hereditary Sensory Autonomic Neuropathy, Type 1
Hereditary Sensory Autonomic Neuropathy, Type 1 		32 0 1 2.3E-02 0 0
CUI: C0238651
Disease: Ankle clonus
Ankle clonus 		32 0 1 2.3E-02 0 0
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense 		33 0 1 2.3E-02 0 0
CUI: C0013312
Disease: Dupuytren Contracture
Dupuytren Contracture 		34 0 1 2.2E-02 0 0
CUI: C1692886
Disease: Arthritis, Bacterial
Arthritis, Bacterial 		34 0 1 2.2E-02 0 0
CUI: C4553976
Disease: Urinary Urgency, CTCAE 5
Urinary Urgency, CTCAE 5 		34 0 1 2.2E-02 0 0