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: C0004134
Disease: Ataxia
Ataxia
868 0 1 1.2E-03 0 0
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
267 0 1 3.7E-03 0 0
CUI: C0005890
Disease: Body Height
Body Height
1903 0 1 5.3E-04 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism
1261 0 1 7.9E-04 0 0
CUI: C0015300
Disease: Exophthalmos
Exophthalmos
225 0 1 4.4E-03 0 0
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
1037 0 1 9.6E-04 0 0
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
272 0 1 3.7E-03 0 0
Sensorineural Hearing Loss (disorder)
783 0 1 1.3E-03 0 0
CUI: C0019214
Disease: Hepatosplenomegaly
Hepatosplenomegaly
127 0 1 7.9E-03 0 0
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
489 0 1 2.0E-03 0 0
CUI: C0022107
Disease: Irritable Mood
Irritable Mood
142 0 1 7.0E-03 0 0
CUI: C0025958
Disease: Microcephaly
Microcephaly
1064 0 1 9.4E-04 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism
586 0 1 1.7E-03 0 0
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
197 0 1 5.1E-03 0 0
CUI: C0027947
Disease: Neutropenia
Neutropenia
389 0 1 2.6E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 6.0E-03 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus
833 0 1 1.2E-03 0 0
CUI: C0032927
Disease: Precancerous Conditions
Precancerous Conditions
471 0 1 2.1E-03 0 0
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
546 0 1 1.8E-03 0 0
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
592 0 1 1.7E-03 0 0
CUI: C0086543
Disease: Cataract
Cataract
878 0 1 1.1E-03 0 0
CUI: C0151849
Disease: Alkaline phosphatase raised
Alkaline phosphatase raised
55 0 1 1.8E-02 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 1 1.9E-03 0 0
CUI: C0158731
Disease: Congenital pectus carinatum
Congenital pectus carinatum
138 0 1 7.2E-03 0 0
CUI: C0221354
Disease: Frontal bossing
Frontal bossing
321 0 1 3.1E-03 0 0