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: C0740997
Disease: Anemia, normochromic macrocytic
Anemia, normochromic macrocytic 		1 0 1 1.00 0 0
CUI: C2751479
Disease: Hypoplastic sacral vertebrae
Hypoplastic sacral vertebrae 		1 0 1 1.00 0 0
CUI: C2751481
Disease: Mild radial hypoplasia
Mild radial hypoplasia 		1 0 1 1.00 0 0
CUI: C0265265
Disease: Aase syndrome
Aase syndrome 		2 0 1 0.50 0 0
CUI: C0427032
Disease: Ankle stiff
Ankle stiff 		2 0 1 0.50 0 0
CUI: C1867923
Disease: Posterior column ataxia
Posterior column ataxia 		2 0 1 0.50 0 0
CUI: C2751480
Disease: Hypoplastic coccygeal vertebrae
Hypoplastic coccygeal vertebrae 		2 0 1 0.50 0 0
CUI: C0877221
Disease: Decreased erythroid precursor production
Decreased erythroid precursor production 		3 0 1 0.33 0 0
CUI: C1542667
Disease: Congenital erythroid hypoplasia
Congenital erythroid hypoplasia 		3 0 1 0.33 0 0
CUI: C2673892
Disease: Ductal plate malformation
Ductal plate malformation 		3 0 1 0.33 0 0
CUI: C4022547
Disease: Elevated red cell adenosine deaminase activity
Elevated red cell adenosine deaminase activity 		3 0 1 0.33 0 0
CUI: C0158995
Disease: Congenital anemia
Congenital anemia 		7 0 1 0.14 0 0
CUI: C1855229
Disease: Spondylometaphyseal dysplasia, Sedaghatian type
Spondylometaphyseal dysplasia, Sedaghatian type 		7 0 1 0.14 0 0
CUI: C0349251
Disease: Behavioral syndrome associated with physiological disturbance and physical factors
Behavioral syndrome associated with physiological disturbance and physical factors 		8 0 1 0.12 0 0
CUI: C0949116
Disease: Congenital hypoplastic anemia
Congenital hypoplastic anemia 		8 0 1 0.12 0 0
CUI: C1853666
Disease: Anemia, Diamond-Blackfan, 2
Anemia, Diamond-Blackfan, 2 		8 0 1 0.12 0 0
CUI: C0231706
Disease: Circling gait
Circling gait 		9 0 1 0.11 0 0
CUI: C0423319
Disease: Atrophic iris
Atrophic iris 		9 0 1 0.11 0 0
CUI: C0741237
Disease: arthritis symptoms
arthritis symptoms 		9 0 1 0.11 0 0
CUI: C0242490
Disease: Enthesopathy
Enthesopathy 		11 0 1 9.1E-02 0 0
CUI: C2986691
Disease: Inherited bone marrow failure syndrome
Inherited bone marrow failure syndrome 		11 0 1 9.1E-02 0 0
CUI: C0022738
Disease: Klippel-Feil Syndrome
Klippel-Feil Syndrome 		12 0 1 8.3E-02 0 0
CUI: C1536075
Disease: Sudden unexplained death in epilepsy
Sudden unexplained death in epilepsy 		12 0 1 8.3E-02 0 0
CUI: C2676137
Disease: Diamond-Blackfan Anemia 1
Diamond-Blackfan Anemia 1 		12 0 1 8.3E-02 0 0
CUI: C4082168
Disease: Partial duplication of thumb phalanx
Partial duplication of thumb phalanx 		12 0 1 8.3E-02 0 0