Source: ALL
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: 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
CUI: C1846492
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4
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
CUI: C1860268
Disease: Gonadal tissue inappropriate for external genitalia or chromosomal sex
Gonadal tissue inappropriate for external genitalia or chromosomal sex 		1 0 1 5.9E-02 0 0
CUI: C3149223
Disease: Aplasia of the abdominal wall musculature
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
CUI: C3540094
Disease: INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 		1 0 1 5.9E-02 0 0
CUI: C3553493
Disease: SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
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
CUI: C0158371
Disease: Acute osteomyelitis
Acute osteomyelitis 		2 0 1 5.6E-02 0 0
CUI: C0270202
Disease: Hemolytic disease of fetus OR newborn due to ABO immunization
Hemolytic disease of fetus OR newborn due to ABO immunization 		2 0 1 5.6E-02 0 0
CUI: C0995195
Disease: Anoxia of brain
Anoxia of brain 		2 0 1 5.6E-02 0 0
CUI: C1140716
Disease: Hypoxic Brain Damage
Hypoxic Brain Damage 		2 0 1 5.6E-02 0 0
CUI: C4024632
Disease: Gonadal dysgenesis with female appearance, male
Gonadal dysgenesis with female appearance, male 		2 0 1 5.6E-02 0 0