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: C3279904
Disease: Lactate Dehydrogenase B Deficiency
Lactate Dehydrogenase B Deficiency
3 0 1 9.1E-02 0 0
CUI: C3874374
Disease: Oncovirus infection
Oncovirus infection
3 0 1 9.1E-02 0 0
CUI: C3887667
Disease: Retrocollis
Retrocollis
3 0 1 9.1E-02 0 0
CUI: C4021300
Disease: Prominent palatine ridges
Prominent palatine ridges
3 0 1 9.1E-02 0 0
CUI: C4021805
Disease: Abnormality of the nasal bridge
Abnormality of the nasal bridge
3 0 1 9.1E-02 0 0
Iron accumulation in substantia nigra
3 0 1 9.1E-02 0 0
Iron accumulation in globus pallidus
3 0 1 9.1E-02 0 0
CUI: C4531083
Disease: Mucinous gastric carcinoma
Mucinous gastric carcinoma
15 0 2 9.1E-02 0 0
Gatad2b associated neurodevelopmental disorder
3 0 1 9.1E-02 0 0
CUI: C0016807
Disease: Functional disorder of intestine
Functional disorder of intestine
4 0 1 8.3E-02 0 0
CUI: C0154856
Disease: Retinal lattice degeneration
Retinal lattice degeneration
4 0 1 8.3E-02 0 0
Narrowing of intervertebral disc space
4 0 1 8.3E-02 0 0
CUI: C1883694
Disease: Intraocular Medulloepithelioma
Intraocular Medulloepithelioma
4 0 1 8.3E-02 0 0
CUI: C4073132
Disease: Abnormal pelvis bone morphology
Abnormal pelvis bone morphology
4 0 1 8.3E-02 0 0
CUI: C1096293
Disease: Macroangiopathy
Macroangiopathy
31 0 3 8.1E-02 0 0
CUI: C1954751
Disease: Microdeletion syndromes
Microdeletion syndromes
18 0 2 8.0E-02 0 0
CUI: C1859212
Disease: Limited neck range of motion
Limited neck range of motion
5 0 1 7.7E-02 0 0
CUI: C1859979
Disease: Precocious puberty in males
Precocious puberty in males
5 0 1 7.7E-02 0 0
Undifferentiated spindle cell sarcoma
5 0 1 7.7E-02 0 0
CUI: C4074771
Disease: Sterility, Reproductive
Sterility, Reproductive
5 0 1 7.7E-02 0 0
CUI: C1834664
Disease: Nasal, dysarthic speech
Nasal, dysarthic speech
6 0 1 7.1E-02 0 0
Transposition of the Great Arteries, Dextro-Looped 1
6 0 1 7.1E-02 0 0
CUI: C1856202
Disease: U-Shaped upper lip vermilion
U-Shaped upper lip vermilion
6 0 1 7.1E-02 0 0
CUI: C4022153
Disease: Cerebral cortical hemiatrophy
Cerebral cortical hemiatrophy
6 0 1 7.1E-02 0 0
CUI: C4728082
Disease: Severe hypoglycaemia
Severe hypoglycaemia
36 0 3 7.1E-02 0 0