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: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms
1 0 1 1.3E-02 0 0
CUI: C0020039
Disease: Hostility
Hostility
1 0 1 1.3E-02 0 0
CUI: C0021177
Disease: Increased Libido
Increased Libido
1 0 1 1.3E-02 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention
1 0 1 1.3E-02 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing
1 0 1 1.3E-02 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal
1 0 1 1.3E-02 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma
1 0 1 1.3E-02 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia
1 1 1 1.3E-02 1 0.11
CUI: C0154695
Disease: Diplegic Infantile Cerebral Palsy
Diplegic Infantile Cerebral Palsy
1 0 1 1.3E-02 0 0
Cerebral Palsy, Quadriplegic, Infantile
1 0 1 1.3E-02 0 0
CUI: C0154698
Disease: Monoplegic Infantile Cerebral Palsy
Monoplegic Infantile Cerebral Palsy
1 0 1 1.3E-02 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis
1 0 1 1.3E-02 0 0
CUI: C0221151
Disease: Projectile vomiting
Projectile vomiting
1 0 1 1.3E-02 0 0
CUI: C0234461
Disease: aphasic
aphasic
1 0 1 1.3E-02 0 0
CUI: C0234516
Disease: Speech dysfunction
Speech dysfunction
1 0 1 1.3E-02 0 0
CUI: C0238014
Disease: Acute cerebellar ataxia
Acute cerebellar ataxia
1 0 1 1.3E-02 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing
1 0 1 1.3E-02 0 0
CUI: C0264725
Disease: Acute left-sided heart failure
Acute left-sided heart failure
1 0 1 1.3E-02 0 0
CUI: C0270807
Disease: Monoplegic Cerebral Palsy
Monoplegic Cerebral Palsy
1 0 1 1.3E-02 0 0
CUI: C0271616
Disease: Precocious female puberty
Precocious female puberty
1 0 1 1.3E-02 0 0
CUI: C0278600
Disease: Childhood Brain Stem Glioma
Childhood Brain Stem Glioma
1 0 1 1.3E-02 0 0
CUI: C0302323
Disease: Reticulohistiocytosis
Reticulohistiocytosis
1 0 1 1.3E-02 0 0
CUI: C0340007
Disease: Catamenial pneumothorax
Catamenial pneumothorax
1 0 1 1.3E-02 0 0
CUI: C0349533
Disease: Lymphoma of intestine
Lymphoma of intestine
1 0 1 1.3E-02 0 0
Benign Neonatal Epilepsy, Nonfamilial
1 0 1 1.3E-02 0 0