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: C4024923
Disease: Diffuse white matter abnormalities
Diffuse white matter abnormalities 		34 0 3 6.4E-02 0 0
CUI: C0342826
Disease: 3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency 		1 0 1 6.2E-02 0 0
CUI: C0410654
Disease: Instability of atlantooccipital joint
Instability of atlantooccipital joint 		1 0 1 6.2E-02 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia 		1 0 1 6.2E-02 0 0
CUI: C0549651
Disease: Abnormality of the lens
Abnormality of the lens 		1 0 1 6.2E-02 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis 		1 0 1 6.2E-02 0 0
CUI: C0796046
Disease: Gurrieri Sammito Bellussi syndrome
Gurrieri Sammito Bellussi syndrome 		1 0 1 6.2E-02 0 0
CUI: C0796124
Disease: Proud Syndrome
Proud Syndrome 		1 0 1 6.2E-02 0 0
CUI: C1096121
Disease: Skeleton dysplasia
Skeleton dysplasia 		1 0 1 6.2E-02 0 0
CUI: C1516419
Disease: Cervical Mesonephric Adenocarcinoma
Cervical Mesonephric Adenocarcinoma 		1 0 1 6.2E-02 0 0
CUI: C1516974
Disease: Estrogen Receptor Status - Clinical Trial Eligibility Criteria
Estrogen Receptor Status - Clinical Trial Eligibility Criteria 		1 0 1 6.2E-02 0 0
CUI: C1517658
Disease: Cervical Keratinizing Squamous Cell Carcinoma
Cervical Keratinizing Squamous Cell Carcinoma 		1 0 1 6.2E-02 0 0
CUI: C1846171
Disease: Lissencephaly, X-Linked, 2
Lissencephaly, X-Linked, 2 		1 0 1 6.2E-02 0 0
CUI: C1846172
Disease: Hydranencephaly and Abnormal Genitalia
Hydranencephaly and Abnormal Genitalia 		1 0 1 6.2E-02 0 0
CUI: C1852407
Disease: Prominent scrotal raphe
Prominent scrotal raphe 		1 0 1 6.2E-02 0 0
CUI: C1852411
Disease: Preauricular skin furrow
Preauricular skin furrow 		1 0 1 6.2E-02 0 0
CUI: C1855305
Disease: Ter Haar syndrome
Ter Haar syndrome 		1 0 1 6.2E-02 0 0
CUI: C1855849
Disease: Bartter syndrome, antenatal , type 2
Bartter syndrome, antenatal , type 2 		1 0 1 6.2E-02 0 0
CUI: C1856911
Disease: Ivory epiphyses
Ivory epiphyses 		1 0 1 6.2E-02 0 0
CUI: C1859406
Disease: Borrone Di Rocco Crovato syndrome
Borrone Di Rocco Crovato syndrome 		1 0 1 6.2E-02 0 0
CUI: C1859478
Disease: Hypoplasia of proximal fibula
Hypoplasia of proximal fibula 		1 0 1 6.2E-02 0 0
CUI: C1863392
Disease: Abnormal morphology of the limbic system
Abnormal morphology of the limbic system 		1 0 1 6.2E-02 0 0
CUI: C1863395
Disease: Acrobrachycephaly
Acrobrachycephaly 		1 0 1 6.2E-02 0 0
CUI: C1863403
Disease: Broad distal hallux
Broad distal hallux 		1 0 1 6.2E-02 0 0
CUI: C1865070
Disease: SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION
SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION 		1 0 1 6.2E-02 0 0