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: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome 		1 0 1 5.6E-02 0 0
CUI: C0265974
Disease: Birthmark
Birthmark 		1 0 1 5.6E-02 0 0
CUI: C0266094
Disease: Congenital macrocheilia
Congenital macrocheilia 		1 0 1 5.6E-02 0 0
CUI: C0267024
Disease: Hypertrophy of lip
Hypertrophy of lip 		1 0 1 5.6E-02 0 0
CUI: C0332972
Disease: Congenital vascular proliferation
Congenital vascular proliferation 		1 0 1 5.6E-02 0 0
CUI: C0332977
Disease: Congenital hemangiomatosis
Congenital hemangiomatosis 		1 0 1 5.6E-02 0 0
CUI: C0349623
Disease: Primary Melanocytic Lesion of Meninges
Primary Melanocytic Lesion of Meninges 		1 0 1 5.6E-02 0 0
CUI: C0522035
Disease: Edema of the upper extremity
Edema of the upper extremity 		1 0 1 5.6E-02 0 0
CUI: C0563632
Disease: Manifest-latent nystagmus
Manifest-latent nystagmus 		1 0 1 5.6E-02 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 5.6E-02 0 0
CUI: C0751402
Disease: Optic Disk Disorders
Optic Disk Disorders 		1 0 1 5.6E-02 0 0
CUI: C1301356
Disease: Refractory cytopenia with multilineage dysplasia and ringed sideroblasts
Refractory cytopenia with multilineage dysplasia and ringed sideroblasts 		1 0 1 5.6E-02 0 0
CUI: C1392110
Disease: Crystalline cataract
Crystalline cataract 		1 0 1 5.6E-02 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 5.6E-02 0 0
CUI: C1837023
Disease: CATARACT, CONGENITAL, CERULEAN TYPE, 3
CATARACT, CONGENITAL, CERULEAN TYPE, 3 		1 0 1 5.6E-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 5.6E-02 0 0
CUI: C1837317
Disease: Alpha-B Crystallinopathy
Alpha-B Crystallinopathy 		1 0 1 5.6E-02 0 0
CUI: C1840347
Disease: HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder)
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder) 		1 0 1 5.6E-02 0 0
CUI: C1847507
Disease: Paroxysmal lethargy
Paroxysmal lethargy 		1 0 1 5.6E-02 0 0
CUI: C1850039
Disease: Pericardial Effusion, Chronic
Pericardial Effusion, Chronic 		1 0 1 5.6E-02 0 0
CUI: C1852429
Disease: Cataract, Variable Zonular Pulverulent
Cataract, Variable Zonular Pulverulent 		1 0 1 5.6E-02 0 0
CUI: C1861832
Disease: CATARACT, CRYSTALLINE ACULEIFORM
CATARACT, CRYSTALLINE ACULEIFORM 		1 0 1 5.6E-02 0 0
CUI: C1866078
Disease: Cataract, Zonular Pulverulent 3
Cataract, Zonular Pulverulent 3 		1 0 1 5.6E-02 0 0
CUI: C1969032
Disease: Cataract, Autosomal Dominant, Multiple Types 1
Cataract, Autosomal Dominant, Multiple Types 1 		1 0 1 5.6E-02 0 0
CUI: C1969644
Disease: Cataract, Cortical, Juvenile-Onset
Cataract, Cortical, Juvenile-Onset 		1 0 1 5.6E-02 0 0