Source: INFERRED ×
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: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 1.4E-03 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 0 1 1.4E-03 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 0 1 1.4E-03 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 1.4E-03 0 0
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		1 0 1 1.4E-03 0 0
CUI: C0205770
Disease: Choroid Plexus Papilloma
Choroid Plexus Papilloma 		1 0 1 1.4E-03 0 0
CUI: C0206657
Disease: Alveolar Soft Part Sarcoma
Alveolar Soft Part Sarcoma 		1 0 1 1.4E-03 0 0
CUI: C0221169
Disease: Hemiballismus
Hemiballismus 		1 0 1 1.4E-03 0 0
CUI: C0238122
Disease: Fallopian Tube Carcinoma
Fallopian Tube Carcinoma 		1 0 1 1.4E-03 0 0
CUI: C0238461
Disease: Anaplastic thyroid carcinoma
Anaplastic thyroid carcinoma 		1 0 1 1.4E-03 0 0
CUI: C0239957
Disease: Hip stiff
Hip stiff 		1 0 1 1.4E-03 0 0
CUI: C0240995
Disease: Increased serum androstenedione
Increased serum androstenedione 		1 0 1 1.4E-03 0 0
CUI: C0242528
Disease: Azotemia
Azotemia 		1 0 1 1.4E-03 0 0
CUI: C0262918
Disease: Extraocular Muscle Paresis
Extraocular Muscle Paresis 		1 0 1 1.4E-03 0 0
CUI: C0265211
Disease: Marshall-Smith syndrome
Marshall-Smith syndrome 		1 0 1 1.4E-03 0 0
CUI: C0265246
Disease: Townes syndrome
Townes syndrome 		1 0 1 1.4E-03 0 0
CUI: C0265338
Disease: Coffin-Siris syndrome
Coffin-Siris syndrome 		1 0 1 1.4E-03 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 0 1 1.4E-03 0 0
CUI: C0266166
Disease: Congenital duplication of intestine
Congenital duplication of intestine 		1 0 1 1.4E-03 0 0
CUI: C0266357
Disease: Persistent umbilical sinus
Persistent umbilical sinus 		1 0 1 1.4E-03 0 0
CUI: C0268532
Disease: Deficiency of prolidase
Deficiency of prolidase 		1 0 1 1.4E-03 0 0
CUI: C0268581
Disease: Holocarboxylase Synthetase Deficiency
Holocarboxylase Synthetase Deficiency 		1 0 1 1.4E-03 0 0
CUI: C0270724
Disease: Infantile Neuroaxonal Dystrophy
Infantile Neuroaxonal Dystrophy 		1 0 1 1.4E-03 0 0
CUI: C0271980
Disease: beta^0^ Thalassemia
beta^0^ Thalassemia 		1 0 1 1.4E-03 0 0
CUI: C0333454
Disease: Granulovacuolar degeneration
Granulovacuolar degeneration 		1 0 1 1.4E-03 0 0