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: C0003119
Disease: Anophthalmos
Anophthalmos
89 0 1 1.1E-02 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity
113 0 1 8.8E-03 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
725 0 1 1.4E-03 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome
137 0 1 7.3E-03 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma
770 0 1 1.3E-03 0 0
CUI: C0018051
Disease: Gonadal Dysgenesis
Gonadal Dysgenesis
53 0 1 1.9E-02 0 0
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
473 0 1 2.1E-03 0 0
CUI: C0025958
Disease: Microcephaly
Microcephaly
1064 0 1 9.4E-04 0 0
CUI: C0026010
Disease: Microphthalmos
Microphthalmos
337 0 1 3.0E-03 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
967 0 1 1.0E-03 0 0
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy
280 0 1 3.6E-03 0 0
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects
304 0 1 3.3E-03 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy
568 0 1 1.8E-03 0 0
CUI: C0035305
Disease: Retinal Detachment
Retinal Detachment
148 0 1 6.8E-03 0 0
CUI: C0035313
Disease: Retinal Dysplasia
Retinal Dysplasia
34 0 1 2.9E-02 0 0
CUI: C0036572
Disease: Seizures
Seizures
2152 0 1 4.6E-04 0 0
CUI: C0086543
Disease: Cataract
Cataract
878 0 1 1.1E-03 0 0
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness
536 0 1 1.9E-03 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia
312 0 1 3.2E-03 0 0
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum
615 0 1 1.6E-03 0 0
CUI: C0221355
Disease: Macrocephaly
Macrocephaly
367 0 1 2.7E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 5.0E-03 0 0
CUI: C0239234
Disease: Low set ears
Low set ears
489 0 1 2.0E-03 0 0
CUI: C0240063
Disease: Coloboma of iris
Coloboma of iris
153 0 1 6.5E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
237 0 1 4.2E-03 0 0