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: C0019489
Disease: Deficiency, Hexosediphosphatase
Deficiency, Hexosediphosphatase 		1 0 1 3.2E-02 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 3.2E-02 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 3.2E-02 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 3.2E-02 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 3.2E-02 0 0
CUI: C0038131
Disease: Stammering
Stammering 		1 0 1 3.2E-02 0 0
CUI: C0042818
Disease: Visual discomfort
Visual discomfort 		1 0 1 3.2E-02 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 3.2E-02 0 0
CUI: C0264487
Disease: Chronic nonspecific lung disease
Chronic nonspecific lung disease 		1 0 1 3.2E-02 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing 		1 0 1 3.2E-02 0 0
CUI: C0454542
Disease: Stuttering, Acquired
Stuttering, Acquired 		1 0 1 3.2E-02 0 0
CUI: C0477972
Disease: Other specified congenital malformations of brain
Other specified congenital malformations of brain 		1 0 1 3.2E-02 0 0
CUI: C0585540
Disease: Myoclonus, Oculopalatal
Myoclonus, Oculopalatal 		1 0 1 3.2E-02 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 3.2E-02 0 0
CUI: C0751348
Disease: Myoclonus Simplex
Myoclonus Simplex 		1 0 1 3.2E-02 0 0
CUI: C0751350
Disease: Myoclonus, Lower Extremity
Myoclonus, Lower Extremity 		1 0 1 3.2E-02 0 0
CUI: C0751351
Disease: Myoclonus, Segmental
Myoclonus, Segmental 		1 0 1 3.2E-02 0 0
CUI: C0751352
Disease: Myoclonus, Nocturnal
Myoclonus, Nocturnal 		1 0 1 3.2E-02 0 0
CUI: C0751353
Disease: Myoclonus, Upper Extremity
Myoclonus, Upper Extremity 		1 0 1 3.2E-02 0 0
CUI: C0751527
Disease: Stuttering, Adult
Stuttering, Adult 		1 0 1 3.2E-02 0 0
CUI: C0855389
Disease: Renin decreased
Renin decreased 		1 0 1 3.2E-02 0 0
CUI: C1389901
Disease: Biotin-dependent carboxylase deficiency, unspecified
Biotin-dependent carboxylase deficiency, unspecified 		1 0 1 3.2E-02 0 0
CUI: C1510417
Disease: Gait Apraxia
Gait Apraxia 		1 0 1 3.2E-02 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 3.2E-02 0 0
CUI: C1837206
Disease: Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly
Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly 		1 0 1 3.2E-02 0 0