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: C0751529
Disease: Stuttering, Developmental
Stuttering, Developmental
13 4 5 0.12 3 0.33
CUI: C0920296
Disease: Developmental reading disorder
Developmental reading disorder
33 0 7 0.12 0 0
CUI: C0454651
Disease: Specific language impairment
Specific language impairment
34 0 6 9.7E-02 0 0
CUI: C0476254
Disease: Dyslexia
Dyslexia
118 0 13 9.4E-02 0 0
CUI: C0007815
Disease: Cerebrospinal Fluid Rhinorrhea
Cerebrospinal Fluid Rhinorrhea
3 0 3 8.8E-02 0 0
CUI: C0751528
Disease: Stuttering, Childhood
Stuttering, Childhood
3 2 3 8.8E-02 1 0.11
MUCOLIPIDOSIS II ALPHA/BETA (disorder)
3 0 3 8.8E-02 0 0
CUI: C0751731
Disease: Intracranial Hypotension, Essential
Intracranial Hypotension, Essential
4 0 3 8.6E-02 0 0
CUI: C0026697
Disease: Mucolipidoses
Mucolipidoses
19 0 4 8.2E-02 0 0
CUI: C1260880
Disease: Rhinorrhea
Rhinorrhea
19 0 4 8.2E-02 0 0
CUI: C0033788
Disease: Pseudo-Hurler Polydystrophy
Pseudo-Hurler Polydystrophy
7 0 3 7.9E-02 0 0
CUI: C0264162
Disease: Camptocormia
Camptocormia
8 0 3 7.7E-02 0 0
CUI: C0221169
Disease: Hemiballismus
Hemiballismus
9 0 3 7.5E-02 0 0
Congenital malformation of corpus callosum
9 0 3 7.5E-02 0 0
CUI: C1847651
Disease: Rapidly progressive dementia
Rapidly progressive dementia
9 0 3 7.5E-02 0 0
CUI: C0149645
Disease: Cervical myelopathy
Cervical myelopathy
12 0 3 7.0E-02 0 0
CUI: C0751699
Disease: Minimally Conscious State
Minimally Conscious State
12 0 3 7.0E-02 0 0
CUI: C4082769
Disease: Chronic Traumatic Encephalopathy
Chronic Traumatic Encephalopathy
12 0 3 7.0E-02 0 0
Anti-N-Methyl-D-Aspartate Receptor Encephalitis
43 0 5 6.9E-02 0 0
CUI: C0001614
Disease: Adrenal Cortex Diseases
Adrenal Cortex Diseases
13 0 3 6.8E-02 0 0
CUI: C0009460
Disease: Communication impairment
Communication impairment
13 0 3 6.8E-02 0 0
CUI: C0595905
Disease: cortex bone disorders
cortex bone disorders
13 0 3 6.8E-02 0 0
CUI: C1264606
Disease: Persistent infection
Persistent infection
13 0 3 6.8E-02 0 0
CUI: C0275544
Disease: Congenital infectious disease
Congenital infectious disease
29 0 4 6.8E-02 0 0
CUI: C0393626
Disease: Opsoclonus-Myoclonus Syndrome
Opsoclonus-Myoclonus Syndrome
14 0 3 6.7E-02 0 0