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: C0268561
Disease: Hyperglycinemia, Nonketotic, Type I
Hyperglycinemia, Nonketotic, Type I
3 0 3 0.14 0 0
Hyperglycinemia, Nonketotic, Type II
3 0 3 0.14 0 0
CUI: C0744897
Disease: Recurrent singultus
Recurrent singultus
3 0 3 0.14 0 0
Hyperglycinemia, Nonketotic, Type III
3 0 3 0.14 0 0
CUI: C0268559
Disease: Hyperglycinemia
Hyperglycinemia
14 0 4 0.13 0 0
CUI: C0268560
Disease: Hyperglycinemia, Transient Neonatal
Hyperglycinemia, Transient Neonatal
2 0 2 9.5E-02 0 0
CUI: C0543541
Disease: HYPERGLYCINURIA (disorder)
HYPERGLYCINURIA (disorder)
14 0 3 9.4E-02 0 0
CUI: C0265428
Disease: Chromosome 9, partial trisomy 9p
Chromosome 9, partial trisomy 9p
4 0 2 8.7E-02 0 0
Delayed ischaemic neurological deficit
4 0 2 8.7E-02 0 0
Disorder of the genitourinary system
5 0 2 8.3E-02 0 0
CUI: C0795830
Disease: CHROMOSOME 9p DELETION SYNDROME
CHROMOSOME 9p DELETION SYNDROME
5 0 2 8.3E-02 0 0
CUI: C2921125
Disease: Post traumatic seizures
Post traumatic seizures
8 0 2 7.4E-02 0 0
CUI: C0002623
Disease: Post-traumatic amnesia
Post-traumatic amnesia
9 0 2 7.1E-02 0 0
CUI: C3887612
Disease: Psychomotor Agitation
Psychomotor Agitation
26 0 3 6.8E-02 0 0
CUI: C0016397
Disease: Focal Infection
Focal Infection
11 0 2 6.7E-02 0 0
CUI: C0393786
Disease: Trigeminal Neuralgia, Idiopathic
Trigeminal Neuralgia, Idiopathic
12 0 2 6.5E-02 0 0
CUI: C0393787
Disease: Secondary Trigeminal Neuralgia
Secondary Trigeminal Neuralgia
12 0 2 6.5E-02 0 0
CUI: C2363866
Disease: Traumatic occlusion
Traumatic occlusion
15 0 2 5.9E-02 0 0
Decreased activity of mitochondrial respiratory chain
34 0 3 5.8E-02 0 0
CUI: C0343532
Disease: Streptococcal toxic shock syndrome
Streptococcal toxic shock syndrome
16 0 2 5.7E-02 0 0
Decreased activity of the pyruvate dehydrogenase complex
35 0 3 5.7E-02 0 0
CUI: C0236075
Disease: Menopausal symptom
Menopausal symptom
17 0 2 5.6E-02 0 0
CUI: C4725024
Disease: Refractory Leukemia
Refractory Leukemia
17 0 2 5.6E-02 0 0
PREMATURE CHROMATID SEPARATION TRAIT
19 0 2 5.3E-02 0 0
CUI: C1837388
Disease: Abnormal pattern of respiration
Abnormal pattern of respiration
20 0 2 5.1E-02 0 0