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: C3805879
Disease: PRECOCIOUS PUBERTY, CENTRAL, 1
PRECOCIOUS PUBERTY, CENTRAL, 1
1 0 1 0.20 0 0
EXUDATIVE VITREORETINOPATHY 4, AUTOSOMAL DOMINANT
1 0 1 0.20 0 0
EXUDATIVE VITREORETINOPATHY 4, AUTOSOMAL RECESSIVE
1 0 1 0.20 0 0
EXUDATIVE VITREORETINOPATHY 4, DIGENIC
1 0 1 0.20 0 0
HYPOGONADOTROPIC HYPOGONADISM 8 WITHOUT ANOSMIA
1 0 1 0.20 0 0
Abnormality of the femoral neck or head region
1 0 1 0.20 0 0
Visual acuity light perception with projection
1 0 1 0.20 0 0
CUI: C4280905
Disease: Degenerative scoliosis
Degenerative scoliosis
1 0 1 0.20 0 0
POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS
1 0 1 0.20 0 0
POLYCYSTIC LIVER DISEASE 4 WITH KIDNEY CYSTS
1 0 1 0.20 0 0
Hormone Receptor Positive Breast Carcinoma
1 0 1 0.20 0 0
CUI: C1291557
Disease: Deficiency of lyase
Deficiency of lyase
8 0 2 0.18 0 0
CUI: C0008352
Disease: Cholemia
Cholemia
2 0 1 0.17 0 0
CUI: C0016696
Disease: Freemartin
Freemartin
2 0 1 0.17 0 0
CUI: C0233767
Disease: Hallucinations, Tactile
Hallucinations, Tactile
2 0 1 0.17 0 0
CUI: C0233949
Disease: Sexual nondevelopment
Sexual nondevelopment
2 0 1 0.17 0 0
CUI: C0242341
Disease: Sexual Infantilism
Sexual Infantilism
2 0 1 0.17 0 0
CUI: C0266981
Disease: Torus palatinus
Torus palatinus
2 0 1 0.17 0 0
Leiomyomatosis peritonealis disseminata
2 0 1 0.17 0 0
CUI: C0271004
Disease: Absent anterior chamber of eye
Absent anterior chamber of eye
2 0 1 0.17 0 0
CUI: C0271614
Disease: Residual ovary syndrome
Residual ovary syndrome
2 0 1 0.17 0 0
CUI: C0311357
Disease: ovarian cystic disease
ovarian cystic disease
2 0 1 0.17 0 0
Impaired glucose tolerance in pregnancy
2 0 1 0.17 0 0
CUI: C0431649
Disease: Vaginal septum
Vaginal septum
2 0 1 0.17 0 0
CUI: C0848259
Disease: male puberty
male puberty
2 0 1 0.17 0 0