Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Reduced insulin like growth factor binding protein acid labile subunit level
1 0 1 0.50 0 0
CUI: C1864570
Disease: Insulin insensitivity
Insulin insensitivity
2 0 1 0.33 0 0
CUI: C3151343
Disease: SPINOCEREBELLAR ATAXIA 32
SPINOCEREBELLAR ATAXIA 32
2 0 1 0.33 0 0
CUI: C0032586
Disease: Polyradiculopathy
Polyradiculopathy
3 0 1 0.25 0 0
CUI: C0349390
Disease: Non-fluent aphasia
Non-fluent aphasia
4 0 1 0.20 0 0
AMYOTROPHIC LATERAL SCLEROSIS 8 (disorder)
4 0 1 0.20 0 0
Hexosaminidase alpha-Subunit Deficiency (Variant B)
4 0 1 0.20 0 0
CUI: C1850406
Disease: NAVAJO NEUROHEPATOPATHY
NAVAJO NEUROHEPATOPATHY
4 0 1 0.20 0 0
CUI: C2146481
Disease: Bilateral vocal cord paralysis
Bilateral vocal cord paralysis
4 0 1 0.20 0 0
CUI: C0282550
Disease: Persian Gulf Syndrome
Persian Gulf Syndrome
5 0 1 0.17 0 0
CUI: C0917814
Disease: Aphasia, Expressive
Aphasia, Expressive
5 0 1 0.17 0 0
CUI: C3825276
Disease: Stereotyped behavior (Psychiatry)
Stereotyped behavior (Psychiatry)
5 0 1 0.17 0 0
CUI: C1835580
Disease: Mild postnatal growth retardation
Mild postnatal growth retardation
6 0 1 0.14 0 0
CUI: C0393547
Disease: Bulbospinal Neuronopathy
Bulbospinal Neuronopathy
7 0 1 0.12 0 0
Decreased serum insulin-like growth factor 1
9 0 1 1.0E-01 0 0
CUI: C0030442
Disease: Progressive bulbar palsy
Progressive bulbar palsy
10 0 1 9.1E-02 0 0
CUI: C0850024
Disease: Gluten sensitivity
Gluten sensitivity
11 0 1 8.3E-02 0 0
CUI: C0018609
Disease: Hartnup Disease
Hartnup Disease
12 0 1 7.7E-02 0 0
CUI: C0042267
Disease: Vaginitis
Vaginitis
12 0 1 7.7E-02 0 0
CUI: C0393911
Disease: Pure Autonomic Failure
Pure Autonomic Failure
12 0 1 7.7E-02 0 0
CUI: C0392678
Disease: Swallowing problem
Swallowing problem
13 0 1 7.1E-02 0 0
Frontotemporal Dementia With Motor Neuron Disease
13 0 1 7.1E-02 0 0
CUI: C0154671
Disease: Degenerative brain disorder
Degenerative brain disorder
16 0 1 5.9E-02 0 0
CUI: C0917981
Disease: Progressive Muscular Atrophy
Progressive Muscular Atrophy
16 0 1 5.9E-02 0 0
CUI: C4317045
Disease: Gluten intolerance
Gluten intolerance
16 0 1 5.9E-02 0 0