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: C0012684
Disease: Blastocyst Disintegration
Blastocyst Disintegration
7 0 7 1.00 0 0
CUI: C0013937
Disease: Embryo Resorption
Embryo Resorption
7 0 7 1.00 0 0
CUI: C0752350
Disease: Embryo Death
Embryo Death
7 0 7 1.00 0 0
CUI: C0752351
Disease: Embryo Loss
Embryo Loss
11 0 7 0.64 0 0
CUI: C0339352
Disease: Capsular cataract (disorder)
Capsular cataract (disorder)
1 0 1 0.14 0 0
CUI: C0520540
Disease: Rebound hypertension
Rebound hypertension
1 0 1 0.14 0 0
CUI: C1855230
Disease: Focal lissencephaly
Focal lissencephaly
1 0 1 0.14 0 0
CUI: C1855240
Disease: Irregular tarsal bones
Irregular tarsal bones
1 0 1 0.14 0 0
Horizontal inferior border of scapula
1 0 1 0.14 0 0
CUI: C4024620
Disease: Widened sacrosciatic notch
Widened sacrosciatic notch
1 0 1 0.14 0 0
CUI: C0036347
Disease: Schizophrenia, Disorganized
Schizophrenia, Disorganized
3 0 1 0.11 0 0
CUI: C1855239
Disease: Cone-shaped metacarpal epiphyses
Cone-shaped metacarpal epiphyses
3 0 1 0.11 0 0
CUI: C1857186
Disease: Iliac crest serration
Iliac crest serration
3 0 1 0.11 0 0
CUI: C2721559
Disease: Osmotic demyelination syndrome
Osmotic demyelination syndrome
3 0 1 0.11 0 0
CUI: C4025828
Disease: Abnormality of the scapula
Abnormality of the scapula
3 0 1 0.11 0 0
CUI: C1848109
Disease: Long fibula
Long fibula
4 0 1 1.0E-01 0 0
CUI: C1855233
Disease: Large posterior fontanelle
Large posterior fontanelle
4 0 1 1.0E-01 0 0
CUI: C1865039
Disease: Cupped ribs
Cupped ribs
4 0 1 1.0E-01 0 0
CUI: C0264652
Disease: Hypertensive heart failure
Hypertensive heart failure
5 0 1 9.1E-02 0 0
CUI: C0451817
Disease: Dietary selenium deficiency
Dietary selenium deficiency
5 0 1 9.1E-02 0 0
CUI: C0457179
Disease: Desmoplastic infantile astrocytoma
Desmoplastic infantile astrocytoma
5 0 1 9.1E-02 0 0
Desmoplastic infantile ganglioglioma
5 0 1 9.1E-02 0 0
Hypertensive left ventricular hypertrophy
5 0 1 9.1E-02 0 0
CUI: C0042875
Disease: Vitamin E Deficiency
Vitamin E Deficiency
6 0 1 8.3E-02 0 0
CUI: C0156372
Disease: Asherman Syndrome
Asherman Syndrome
7 0 1 7.7E-02 0 0