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: C0157733
Disease: Abnormality of the hair
Abnormality of the hair
1 1 1 4.3E-02 1 0.33
Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism
1 0 1 4.3E-02 0 0
CUI: C0405584
Disease: Sucrose intolerance
Sucrose intolerance
1 0 1 4.3E-02 0 0
CUI: C0429803
Disease: Bladder trabeculation
Bladder trabeculation
1 0 1 4.3E-02 0 0
CUI: C0432149
Disease: Lumbar hemivertebra
Lumbar hemivertebra
1 0 1 4.3E-02 0 0
CUI: C0432334
Disease: Inherited cutis laxa
Inherited cutis laxa
1 0 1 4.3E-02 0 0
Congenital supravalvular aortic stenosis
1 0 1 4.3E-02 0 0
CUI: C1333286
Disease: Diencephalic Neoplasm
Diencephalic Neoplasm
1 0 1 4.3E-02 0 0
Serpentine fibula polycystic kidney syndrome
1 0 1 4.3E-02 0 0
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
1 0 1 4.3E-02 0 0
CUI: C1846266
Disease: Laterally curved eyebrow
Laterally curved eyebrow
1 0 1 4.3E-02 0 0
CUI: C1848392
Disease: Zunich neuroectodermal syndrome
Zunich neuroectodermal syndrome
1 0 1 4.3E-02 0 0
CUI: C1855616
Disease: Cartilaginous ossification of nose
Cartilaginous ossification of nose
1 0 1 4.3E-02 0 0
Premature fusion of phalangeal epiphyses
1 0 1 4.3E-02 0 0
Cartilaginous ossification of larynx
1 0 1 4.3E-02 0 0
CUI: C1859366
Disease: Hypoplastic 5th lumbar vertebrae
Hypoplastic 5th lumbar vertebrae
1 0 1 4.3E-02 0 0
Obliteration of the calvarial diploe
1 0 1 4.3E-02 0 0
CUI: C1861627
Disease: Butterfly vertebral arch
Butterfly vertebral arch
1 0 1 4.3E-02 0 0
CUI: C1863012
Disease: Amelogenesis Imperfecta, Type IV
Amelogenesis Imperfecta, Type IV
1 3 1 4.3E-02 1 0.20
CUI: C1863311
Disease: Elongated sella turcica
Elongated sella turcica
1 0 1 4.3E-02 0 0
CUI: C1863313
Disease: Tall lumbar vertebral bodies
Tall lumbar vertebral bodies
1 0 1 4.3E-02 0 0
CUI: C1863314
Disease: Cervical instability
Cervical instability
1 0 1 4.3E-02 0 0
CUI: C1863317
Disease: Crowded carpal bones
Crowded carpal bones
1 0 1 4.3E-02 0 0
Deafness, Congenital Heart Defects, and Posterior Embryotoxon
1 0 1 4.3E-02 0 0
CUI: C2053440
Disease: Thin lower lip vermilion
Thin lower lip vermilion
1 0 1 4.3E-02 0 0