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: C2697779
Disease: Interleukin 2 Measurement
Interleukin 2 Measurement
5 6 2 1.0E-01 2 6.9E-02
CUI: C2825877
Disease: Interferon Gamma Measurement
Interferon Gamma Measurement
5 10 2 1.0E-01 2 6.1E-02
CUI: C0027932
Disease: Neurotic Disorders
Neurotic Disorders
7 0 2 9.1E-02 0 0
CUI: C2825857
Disease: Factor VIII measurement
Factor VIII measurement
15 0 2 6.7E-02 0 0
CUI: C4021972
Disease: Urogenital sinus anomaly
Urogenital sinus anomaly
18 0 2 6.1E-02 0 0
CUI: C0005848
Disease: Blood Viscosity
Blood Viscosity
1 0 1 5.9E-02 0 0
CUI: C0039614
Disease: Tetanus
Tetanus
1 0 1 5.9E-02 0 0
CUI: C0265363
Disease: Urethral obstruction sequence
Urethral obstruction sequence
1 0 1 5.9E-02 0 0
CUI: C0394004
Disease: Congenital non-progressive ataxia
Congenital non-progressive ataxia
1 0 1 5.9E-02 0 0
CUI: C0585556
Disease: Macrosaccadic oscillations
Macrosaccadic oscillations
1 0 1 5.9E-02 0 0
CUI: C0810006
Disease: Acute cerebrovascular disease
Acute cerebrovascular disease
1 0 1 5.9E-02 0 0
CUI: C1319016
Disease: Nephrogenic rest, intralobar
Nephrogenic rest, intralobar
1 0 1 5.9E-02 0 0
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder)
1 0 1 5.9E-02 0 0
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4
1 0 1 5.9E-02 0 0
CUI: C1847725
Disease: SPINOCEREBELLAR ATAXIA 15
SPINOCEREBELLAR ATAXIA 15
1 0 1 5.9E-02 0 0
Gonadal tissue inappropriate for external genitalia or chromosomal sex
1 0 1 5.9E-02 0 0
Aplasia of the abdominal wall musculature
1 0 1 5.9E-02 0 0
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4
1 0 1 5.9E-02 0 0
INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
1 0 1 5.9E-02 0 0
SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
1 0 1 5.9E-02 0 0
CUI: C4274322
Disease: Spinocerebellar ataxia type 15/16
Spinocerebellar ataxia type 15/16
1 0 1 5.9E-02 0 0
CUI: C4324411
Disease: Blood type incompatibility
Blood type incompatibility
1 0 1 5.9E-02 0 0
CUI: C4703482
Disease: Severe Epstein Barr virus infection
Severe Epstein Barr virus infection
1 0 1 5.9E-02 0 0
CUI: C0003132
Disease: Anoxic Encephalopathy
Anoxic Encephalopathy
2 0 1 5.6E-02 0 0
CUI: C0020701
Disease: Hysteria
Hysteria
2 0 1 5.6E-02 0 0