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: C0232466
Disease: Feeding difficulties
Feeding difficulties 		473 0 1 2.1E-03 0 0
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy 		454 0 1 2.2E-03 0 0
CUI: C0239137
Disease: Coxa valga
Coxa valga 		68 0 1 1.5E-02 0 0
CUI: C0239181
Disease: Intermittent diarrhea
Intermittent diarrhea 		17 0 1 5.9E-02 0 0
CUI: C0240538
Disease: Convex nasal ridge
Convex nasal ridge 		69 0 1 1.4E-02 0 0
CUI: C0277959
Disease: Coarse hair
Coarse hair 		60 0 1 1.7E-02 0 0
CUI: C0282313
Disease: Condition, Preneoplastic
Condition, Preneoplastic 		122 0 1 8.2E-03 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		385 0 1 2.6E-03 0 0
CUI: C0426430
Disease: Drooping nasal tip
Drooping nasal tip 		3 0 1 0.33 0 0
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		560 0 1 1.8E-03 0 0
CUI: C0456103
Disease: Sepsis of the newborn
Sepsis of the newborn 		53 0 1 1.9E-02 0 0
CUI: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay 		393 0 1 2.5E-03 0 0
CUI: C0575802
Disease: Small hand
Small hand 		108 0 1 9.3E-03 0 0
CUI: C0581381
Disease: Recurrent upper respiratory tract infection
Recurrent upper respiratory tract infection 		52 0 1 1.9E-02 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 1 2.1E-02 0 0
CUI: C0751057
Disease: Seizure, Febrile, Complex
Seizure, Febrile, Complex 		19 0 1 5.3E-02 0 0
CUI: C1314665
Disease: Serum alkaline phosphatase raised
Serum alkaline phosphatase raised 		67 0 1 1.5E-02 0 0
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		919 0 1 1.1E-03 0 0
CUI: C1837084
Disease: Short metacarpal
Short metacarpal 		66 0 1 1.5E-02 0 0
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay 		118 0 1 8.5E-03 0 0
CUI: C1837785
Disease: Prominent superficial veins
Prominent superficial veins 		8 0 1 0.12 0 0
CUI: C1838391
Disease: Limb hypertonia
Limb hypertonia 		77 0 1 1.3E-02 0 0
CUI: C1842836
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii 		6 0 1 0.17 0 0
CUI: C1843108
Disease: Short palm
Short palm 		110 0 1 9.1E-03 0 0
CUI: C1844704
Disease: Platyspondyly
Platyspondyly 		93 0 1 1.1E-02 0 0