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: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia
216 0 1 2.8E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 2.8E-03 0 0
CUI: C0026499
Disease: Monosomy
Monosomy
214 0 1 2.8E-03 0 0
CUI: C0023269
Disease: leiomyosarcoma
leiomyosarcoma
213 0 1 2.9E-03 0 0
CUI: C1843013
Disease: Alzheimer disease, familial, type 3
Alzheimer disease, familial, type 3
213 0 1 2.9E-03 0 0
CUI: C0730328
Disease: Central Serous Chorioretinopathy
Central Serous Chorioretinopathy
211 0 1 2.9E-03 0 0
CUI: C0035344
Disease: Retinopathy of Prematurity
Retinopathy of Prematurity
202 0 1 2.9E-03 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis
198 0 1 3.0E-03 0 0
Abnormality of cardiovascular system morphology
198 0 1 3.0E-03 0 0
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
197 0 1 3.0E-03 0 0
CUI: C0039103
Disease: Synovitis
Synovitis
197 0 1 3.0E-03 0 0
CUI: C0036920
Disease: Sezary Syndrome
Sezary Syndrome
196 0 1 3.0E-03 0 0
CUI: C0020757
Disease: Ichthyoses
Ichthyoses
194 0 1 3.0E-03 0 0
CUI: C0027626
Disease: Neoplasm Invasiveness
Neoplasm Invasiveness
193 0 1 3.0E-03 0 0
CUI: C0027809
Disease: Neurilemmoma
Neurilemmoma
193 0 1 3.0E-03 0 0
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions
192 0 1 3.0E-03 0 0
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
189 0 1 3.1E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly
186 0 1 3.1E-03 0 0
CUI: C0878500
Disease: Intraepithelial Neoplasia
Intraepithelial Neoplasia
186 0 1 3.1E-03 0 0
CUI: C0026277
Disease: Mixed Salivary Gland Tumor
Mixed Salivary Gland Tumor
185 0 1 3.1E-03 0 0
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
185 0 1 3.1E-03 0 0
CUI: C0262584
Disease: Carcinoma, Small Cell
Carcinoma, Small Cell
185 0 1 3.1E-03 0 0
CUI: C0740858
Disease: Substance abuse problem
Substance abuse problem
185 0 1 3.1E-03 0 0
CUI: C1266042
Disease: Chromophobe Renal Cell Carcinoma
Chromophobe Renal Cell Carcinoma
185 0 1 3.1E-03 0 0
CUI: C0271183
Disease: Severe myopia
Severe myopia
184 0 1 3.1E-03 0 0