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: C0037932
Disease: Curvature of spine
Curvature of spine 		1 0 1 1.4E-02 0 0
CUI: C0157733
Disease: Abnormality of the hair
Abnormality of the hair 		1 0 1 1.4E-02 0 0
CUI: C0241633
Disease: Vaginal dryness
Vaginal dryness 		1 0 1 1.4E-02 0 0
CUI: C0266062
Disease: Posterior open bite
Posterior open bite 		1 0 1 1.4E-02 0 0
CUI: C0266177
Disease: Megaduodenum
Megaduodenum 		1 0 1 1.4E-02 0 0
CUI: C0340031
Disease: Mucociliary clearance defect
Mucociliary clearance defect 		1 0 1 1.4E-02 0 0
CUI: C0342826
Disease: 3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency 		1 0 1 1.4E-02 0 0
CUI: C0342841
Disease: Hunter's syndrome, severe form
Hunter's syndrome, severe form 		1 0 1 1.4E-02 0 0
CUI: C0342842
Disease: Hunter's syndrome, mild form
Hunter's syndrome, mild form 		1 0 1 1.4E-02 0 0
CUI: C0344987
Disease: Bicuspid pulmonary valve
Bicuspid pulmonary valve 		1 0 1 1.4E-02 0 0
CUI: C0399373
Disease: Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism
Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism 		1 0 1 1.4E-02 0 0
CUI: C0410652
Disease: Cervical spine instability
Cervical spine instability 		1 0 1 1.4E-02 0 0
CUI: C0431501
Disease: Bilateral arterial duct
Bilateral arterial duct 		1 0 1 1.4E-02 0 0
CUI: C0478093
Disease: Other congenital malformation syndromes with other skeletal changes
Other congenital malformation syndromes with other skeletal changes 		1 0 1 1.4E-02 0 0
CUI: C0495617
Disease: Congenital scoliosis due to bony malformation
Congenital scoliosis due to bony malformation 		1 0 1 1.4E-02 0 0
CUI: C0521527
Disease: Shortened trunk
Shortened trunk 		1 0 1 1.4E-02 0 0
CUI: C0740850
Disease: airway disease restrictive
airway disease restrictive 		1 0 1 1.4E-02 0 0
CUI: C0741146
Disease: anxiety acute
anxiety acute 		1 0 1 1.4E-02 0 0
CUI: C0741918
Disease: Structural cardiac defects
Structural cardiac defects 		1 0 1 1.4E-02 0 0
CUI: C0795821
Disease: Chromosome 7, trisomy 7q
Chromosome 7, trisomy 7q 		1 0 1 1.4E-02 0 0
CUI: C0795927
Disease: Deafness, congenital onychodystrophy, recessive form
Deafness, congenital onychodystrophy, recessive form 		1 0 1 1.4E-02 0 0
CUI: C0796159
Disease: Mental retardation Smith Fineman Myers type
Mental retardation Smith Fineman Myers type 		1 0 1 1.4E-02 0 0
CUI: C0796182
Disease: Acromelic frontonasal dysplasia
Acromelic frontonasal dysplasia 		1 0 1 1.4E-02 0 0
CUI: C0856823
Disease: Undifferentiated type acute leukemia
Undifferentiated type acute leukemia 		1 0 1 1.4E-02 0 0
CUI: C0860475
Disease: Lactose intolerant
Lactose intolerant 		1 0 1 1.4E-02 0 0