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: C0334491
Disease: Benign Mesenchymoma
Benign Mesenchymoma
1 0 1 9.6E-03 0 0
3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
1 0 1 9.6E-03 0 0
CUI: C0345382
Disease: Gorlin Chaudhry Moss syndrome
Gorlin Chaudhry Moss syndrome
1 0 1 9.6E-03 0 0
CUI: C0349565
Disease: Lipoma of breast
Lipoma of breast
1 0 1 9.6E-03 0 0
CUI: C0410652
Disease: Cervical spine instability
Cervical spine instability
1 0 1 9.6E-03 0 0
Instability of atlantooccipital joint
1 0 1 9.6E-03 0 0
Trichorhinophalangeal dysplasia type I
1 43 1 9.6E-03 1 1.8E-02
CUI: C0578437
Disease: Ischemic foot
Ischemic foot
1 0 1 9.6E-03 0 0
CUI: C0580550
Disease: Lymphocyte count abnormal
Lymphocyte count abnormal
1 0 1 9.6E-03 0 0
CUI: C0741918
Disease: Structural cardiac defects
Structural cardiac defects
1 0 1 9.6E-03 0 0
CUI: C0743515
Disease: endometrial polyp benign
endometrial polyp benign
1 0 1 9.6E-03 0 0
CUI: C0749474
Disease: thyroid nodule solitary
thyroid nodule solitary
1 0 1 9.6E-03 0 0
CUI: C0795821
Disease: Chromosome 7, trisomy 7q
Chromosome 7, trisomy 7q
1 0 1 9.6E-03 0 0
CUI: C0795932
Disease: fontaine syndrome
fontaine syndrome
1 0 1 9.6E-03 0 0
Mental retardation Smith Fineman Myers type
1 0 1 9.6E-03 0 0
CUI: C0796182
Disease: Acromelic frontonasal dysplasia
Acromelic frontonasal dysplasia
1 0 1 9.6E-03 0 0
Acromegaloid facial appearance syndrome
1 0 1 9.6E-03 0 0
CUI: C0809936
Disease: Branchio-skeleto-genital syndrome
Branchio-skeleto-genital syndrome
1 0 1 9.6E-03 0 0
CUI: C0854328
Disease: Infection due to anaerobic bacteria
Infection due to anaerobic bacteria
1 0 1 9.6E-03 0 0
CUI: C0855040
Disease: Epithelioid sarcoma non-metastatic
Epithelioid sarcoma non-metastatic
1 0 1 9.6E-03 0 0
Undifferentiated type acute leukemia
1 0 1 9.6E-03 0 0
Precursor B-lymphoblastic lymphoma stage II
1 0 1 9.6E-03 0 0
CUI: C0865573
Disease: Mitral disease
Mitral disease
1 0 1 9.6E-03 0 0
CUI: C1096121
Disease: Skeleton dysplasia
Skeleton dysplasia
1 0 1 9.6E-03 0 0
CUI: C1257960
Disease: Mannosidase Deficiency Diseases
Mannosidase Deficiency Diseases
1 0 1 9.6E-03 0 0