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: C0003126
Disease: Anosmia
Anosmia
1 0 1 0.17 0 0
CUI: C0007166
Disease: Low Cardiac Output
Low Cardiac Output
1 0 1 0.17 0 0
CUI: C0015930
Disease: Fetal Distress
Fetal Distress
1 0 1 0.17 0 0
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
1 0 1 0.17 0 0
CUI: C0033575
Disease: Prostatic Diseases
Prostatic Diseases
1 0 1 0.17 0 0
CUI: C0553757
Disease: Olfaction Disorders
Olfaction Disorders
1 0 1 0.17 0 0
CUI: C0600177
Disease: Low Cardiac Output Syndrome
Low Cardiac Output Syndrome
1 0 1 0.17 0 0
CUI: C0751325
Disease: Hypertonia, Detrusor Muscle
Hypertonia, Detrusor Muscle
1 0 1 0.17 0 0
CUI: C0751326
Disease: Hypertonia, Infantile
Hypertonia, Infantile
1 0 1 0.17 0 0
CUI: C0751327
Disease: Hypertonia, Neonatal
Hypertonia, Neonatal
1 0 1 0.17 0 0
CUI: C0751328
Disease: Hypertonia, Sphincter
Hypertonia, Sphincter
1 0 1 0.17 0 0
CUI: C0751329
Disease: Hypertonia, Transient
Hypertonia, Transient
1 0 1 0.17 0 0
CUI: C1510410
Disease: Sense of smell altered
Sense of smell altered
1 0 1 0.17 0 0
CUI: C1847604
Disease: Van der Woude syndrome 2
Van der Woude syndrome 2
1 0 1 0.17 0 0
CUI: C3888024
Disease: Cacosmia
Cacosmia
1 0 1 0.17 0 0
IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA
1 0 1 0.17 0 0
Myeloid and/or lymphoid neoplasm associated with platelet derived growth factor receptor alpha rearrangement
1 0 1 0.17 0 0
CUI: C0001122
Disease: Acidosis
Acidosis
2 0 1 0.14 0 0
CUI: C0013390
Disease: Dysmenorrhea
Dysmenorrhea
2 0 1 0.14 0 0
CUI: C0037763
Disease: Spasm
Spasm
2 0 1 0.14 0 0
CUI: C0039338
Disease: Taste Disorders
Taste Disorders
2 0 1 0.14 0 0
CUI: C0043049
Disease: Water Intoxication
Water Intoxication
2 0 1 0.14 0 0
CUI: C0151911
Disease: Generalized Spasms
Generalized Spasms
2 0 1 0.14 0 0
CUI: C0175697
Disease: Van der Woude syndrome
Van der Woude syndrome
2 0 1 0.14 0 0
Idiopathic Hypereosinophilic Syndrome
2 0 1 0.14 0 0