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: C0024950
Disease: Maxillary Diseases
Maxillary Diseases
1 0 1 2.0E-03 0 0
CUI: C0025211
Disease: Conjunctival melanosis
Conjunctival melanosis
1 0 1 2.0E-03 0 0
CUI: C0025467
Disease: Mesenteric Cyst
Mesenteric Cyst
1 0 1 2.0E-03 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing
1 0 1 2.0E-03 0 0
CUI: C0026686
Disease: Mucocele of salivary gland
Mucocele of salivary gland
1 0 1 2.0E-03 0 0
CUI: C0029437
Disease: Idiopathic Multicentric Osteolyses
Idiopathic Multicentric Osteolyses
1 0 1 2.0E-03 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal
1 0 1 2.0E-03 0 0
CUI: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms
1 0 1 2.0E-03 0 0
CUI: C0031085
Disease: Periodontal Abscess
Periodontal Abscess
1 0 1 2.0E-03 0 0
CUI: C0031911
Disease: Pigmentation
Pigmentation
1 0 1 2.0E-03 0 0
CUI: C0034184
Disease: Pyelocystitis
Pyelocystitis
1 0 1 2.0E-03 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma
1 0 1 2.0E-03 0 0
CUI: C0037932
Disease: Curvature of spine
Curvature of spine
1 0 1 2.0E-03 0 0
CUI: C0037942
Disease: Spinal Osteophytosis
Spinal Osteophytosis
1 0 1 2.0E-03 0 0
CUI: C0085313
Disease: Blastocystis Infections
Blastocystis Infections
1 0 1 2.0E-03 0 0
CUI: C0085388
Disease: Intracranial Tuberculoma
Intracranial Tuberculoma
1 0 1 2.0E-03 0 0
CUI: C0149622
Disease: Neurogenic Urinary Bladder, Atonic
Neurogenic Urinary Bladder, Atonic
1 0 1 2.0E-03 0 0
CUI: C0149704
Disease: Gingivostomatitis
Gingivostomatitis
1 0 1 2.0E-03 0 0
Megaloblastic anemia due to folate deficiency
1 0 1 2.0E-03 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome
1 0 1 2.0E-03 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia
1 0 1 2.0E-03 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia
1 1 1 2.0E-03 1 6.0E-03
CUI: C0154834
Disease: Retinal Microaneurysm
Retinal Microaneurysm
1 0 1 2.0E-03 0 0
Acute posterior multifocal placoid pigment epitheliopathy
1 0 1 2.0E-03 0 0
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea
1 0 1 2.0E-03 0 0