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: C0037301
Disease: Skin Wrinkling
Skin Wrinkling
12 0 1 8.3E-02 0 0
CUI: C0003742
Disease: Arcus Senilis
Arcus Senilis
13 0 1 7.7E-02 0 0
CUI: C1389102
Disease: Atrophy of the spinal cord
Atrophy of the spinal cord
13 0 1 7.7E-02 0 0
Spastic paraplegia type 5A, recessive
13 0 1 7.7E-02 0 0
CUI: C0240116
Disease: Hyperactive patellar reflex
Hyperactive patellar reflex
14 0 1 7.1E-02 0 0
CUI: C0422895
Disease: Primitive reflex
Primitive reflex
14 0 1 7.1E-02 0 0
Primitive reflexes (palmomental, snout, glabellar)
14 0 1 7.1E-02 0 0
Complicated hereditary spastic paraplegia
16 0 1 6.2E-02 0 0
CUI: C1843175
Disease: Hyperreflexia in upper limbs
Hyperreflexia in upper limbs
16 0 1 6.2E-02 0 0
CUI: C0080274
Disease: Urinary Retention
Urinary Retention
17 0 1 5.9E-02 0 0
CUI: C0235259
Disease: Subcapsular cataract
Subcapsular cataract
17 0 1 5.9E-02 0 0
CUI: C3665335
Disease: Cutis laxa, autosomal recessive
Cutis laxa, autosomal recessive
17 0 1 5.9E-02 0 0
CUI: C1853377
Disease: Enlarged cisterna magna
Enlarged cisterna magna
18 0 1 5.6E-02 0 0
CUI: C0728829
Disease: Congenital pes cavus
Congenital pes cavus
19 15 1 5.3E-02 1 5.6E-02
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
20 19 1 5.0E-02 1 4.5E-02
Abnormal upper motor neuron morphology
20 0 1 5.0E-02 0 0
CUI: C0431370
Disease: Atrophy of corpus callosum
Atrophy of corpus callosum
21 0 1 4.8E-02 0 0
CUI: C0743332
Disease: Focal Dystonia
Focal Dystonia
21 0 1 4.8E-02 0 0
CUI: C1843885
Disease: Progressive gait ataxia
Progressive gait ataxia
21 0 1 4.8E-02 0 0
CUI: C1845245
Disease: Lower limb hypertonia
Lower limb hypertonia
21 0 1 4.8E-02 0 0
CUI: C3840083
Disease: Late closure of anterior fontanel
Late closure of anterior fontanel
21 0 1 4.8E-02 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls
22 0 1 4.5E-02 0 0
CUI: C0038505
Disease: Sturge-Weber Syndrome
Sturge-Weber Syndrome
25 0 1 4.0E-02 0 0
CUI: C0431369
Disease: Dysgenesis of corpus callosum
Dysgenesis of corpus callosum
25 0 1 4.0E-02 0 0
Hereditary Autosomal Dominant Spastic Paraplegia
27 0 1 3.7E-02 0 0