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: C4025640
Disease: Deficient excision of UV-induced pyrimidine dimers in DNA
Deficient excision of UV-induced pyrimidine dimers in DNA 		4 0 4 1.00 0 0
CUI: C3554724
Disease: Complete duplication of thumb phalanx
Complete duplication of thumb phalanx 		8 0 4 0.50 0 0
CUI: C4021737
Disease: Chromosomal breakage induced by crosslinking agents
Chromosomal breakage induced by crosslinking agents 		8 0 4 0.50 0 0
CUI: C4025811
Disease: Anemic pallor
Anemic pallor 		8 0 4 0.50 0 0
CUI: C2750866
Disease: Growth retardation, pre- and postnatal
Growth retardation, pre- and postnatal 		3 0 2 0.40 0 0
CUI: C1856796
Disease: Estren-Dameshek Variant of Fanconi Anemia
Estren-Dameshek Variant of Fanconi Anemia 		1 0 1 0.25 0 0
CUI: C1856797
Disease: Estren-Dameshek Variant of Fanconi Pancytopenia
Estren-Dameshek Variant of Fanconi Pancytopenia 		1 0 1 0.25 0 0
CUI: C0858867
Disease: Reticulocytopenia
Reticulocytopenia 		17 0 4 0.24 0 0
CUI: C1858565
Disease: Duplicated collecting system
Duplicated collecting system 		19 0 4 0.21 0 0
CUI: C0339637
Disease: Consecutive exotropia
Consecutive exotropia 		2 0 1 0.20 0 0
CUI: C3160739
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP E
FANCONI ANEMIA, COMPLEMENTATION GROUP E 		2 0 1 0.20 0 0
CUI: C3665815
Disease: CYP2B6 polymorphism
CYP2B6 polymorphism 		2 0 1 0.20 0 0
CUI: C0241391
Disease: Thumb absent
Thumb absent 		21 0 4 0.19 0 0
CUI: C3278811
Disease: Thumb aplasia
Thumb aplasia 		22 0 4 0.18 0 0
CUI: C3826743
Disease: Anemia in children
Anemia in children 		9 0 2 0.18 0 0
CUI: C4022016
Disease: Abnormality of the preputium
Abnormality of the preputium 		22 0 4 0.18 0 0
CUI: C4023917
Disease: Aplasia/Hypoplasia of the uvula
Aplasia/Hypoplasia of the uvula 		22 0 4 0.18 0 0
CUI: C4025071
Disease: Aplasia/Hypoplasia of fingers
Aplasia/Hypoplasia of fingers 		22 0 4 0.18 0 0
CUI: C0155336
Disease: Esotropia with accommodative compensation
Esotropia with accommodative compensation 		3 0 1 0.17 0 0
CUI: C0272027
Disease: Pyridoxine-responsive sideroblastic anemia
Pyridoxine-responsive sideroblastic anemia 		24 0 4 0.17 0 0
CUI: C0342526
Disease: Absent testes
Absent testes 		24 0 4 0.17 0 0
CUI: C1405984
Disease: Absent radius
Absent radius 		24 0 4 0.17 0 0
CUI: C4509024
Disease: Senile systemic amyloidosis (SSA)
Senile systemic amyloidosis (SSA) 		3 0 1 0.17 0 0
CUI: C1835817
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP N
FANCONI ANEMIA, COMPLEMENTATION GROUP N 		4 0 1 0.14 0 0
CUI: C0238093
Disease: Stenosis of duodenum
Stenosis of duodenum 		29 0 4 0.14 0 0