Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Neurodegeneration Due To Cerebral Folate Transport Deficiency
8 0 3 7.0E-02 0 0
CUI: C0080174
Disease: Spina Bifida Occulta
Spina Bifida Occulta
76 0 7 6.5E-02 0 0
CUI: C0752235
Disease: Lyme Neuroborreliosis
Lyme Neuroborreliosis
11 0 3 6.5E-02 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 3 6.4E-02 0 0
CUI: C0079770
Disease: Lymphoma, Small Noncleaved-Cell
Lymphoma, Small Noncleaved-Cell
32 0 4 6.1E-02 0 0
CUI: C0426848
Disease: Sacral dimple
Sacral dimple
69 0 6 5.9E-02 0 0
CUI: C0016412
Disease: Folic Acid Deficiency
Folic Acid Deficiency
70 0 6 5.9E-02 0 0
CUI: C0003803
Disease: Arnold Chiari Malformation
Arnold Chiari Malformation
53 0 5 5.8E-02 0 0
CUI: C0426816
Disease: Absence of rib
Absence of rib
18 0 3 5.7E-02 0 0
CUI: C0851886
Disease: Pneumocystis Infections
Pneumocystis Infections
18 0 3 5.7E-02 0 0
CUI: C0027927
Disease: Neurosyphilis
Neurosyphilis
19 0 3 5.6E-02 0 0
CUI: C0020256
Disease: Congenital Hydrocephalus
Congenital Hydrocephalus
39 0 4 5.5E-02 0 0
Slow acetylator due to N-acetyltransferase enzyme variant
20 0 3 5.5E-02 0 0
CUI: C1568868
Disease: Oral Mucositis
Oral Mucositis
59 0 5 5.4E-02 0 0
CUI: C0011268
Disease: Senile dementia
Senile dementia
21 0 3 5.4E-02 0 0
CUI: C0024304
Disease: Lymphoma, Mixed-Cell
Lymphoma, Mixed-Cell
21 0 3 5.4E-02 0 0
CUI: C0079757
Disease: Diffuse Mixed-Cell Lymphoma
Diffuse Mixed-Cell Lymphoma
21 0 3 5.4E-02 0 0
CUI: C0238207
Disease: Ectopic kidney
Ectopic kidney
41 0 4 5.3E-02 0 0
CUI: C0015423
Disease: Eyelid Diseases
Eyelid Diseases
2 0 2 5.3E-02 0 0
CUI: C1867774
Disease: Sacral Agenesis Syndrome
Sacral Agenesis Syndrome
2 0 2 5.3E-02 0 0
CUI: C2609260
Disease: Caudal dysplasia syndrome
Caudal dysplasia syndrome
2 0 2 5.3E-02 0 0
Abnormality of the wing of the ilium
2 0 2 5.3E-02 0 0
CUI: C4706502
Disease: Distal monosomy 13q syndrome
Distal monosomy 13q syndrome
2 0 2 5.3E-02 0 0
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency
43 0 4 5.2E-02 0 0
CUI: C0220810
Disease: Congenital defects
Congenital defects
126 0 8 5.1E-02 0 0