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: C0020623
Disease: Hypolipoproteinemias
Hypolipoproteinemias
1 0 1 0.12 0 0
CUI: C0035326
Disease: Retinal vascular occlusion
Retinal vascular occlusion
1 0 1 0.12 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy
1 0 1 0.12 0 0
CUI: C0162824
Disease: Dermatitis, Photoallergic
Dermatitis, Photoallergic
1 0 1 0.12 0 0
CUI: C0234918
Disease: Morbilliform rash
Morbilliform rash
1 0 1 0.12 0 0
CUI: C0276044
Disease: Contagious bovine pleuropneumonia
Contagious bovine pleuropneumonia
1 0 1 0.12 0 0
CUI: C0339495
Disease: Cilioretinal artery occlusion
Cilioretinal artery occlusion
1 0 1 0.12 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis
1 0 1 0.12 0 0
Hyper-IgD periodic fever syndrome (HIDS)
1 0 1 0.12 0 0
CUI: C1300256
Disease: Thanatophoric dysplasia, type 1
Thanatophoric dysplasia, type 1
1 0 1 0.12 0 0
CUI: C1442958
Disease: Actinic porokeratosis
Actinic porokeratosis
1 0 1 0.12 0 0
CUI: C1720772
Disease: Hypoprebetalipoproteinemia
Hypoprebetalipoproteinemia
1 0 1 0.12 0 0
CUI: C1835362
Disease: Lp(A) Deficiency, Congenital
Lp(A) Deficiency, Congenital
1 0 1 0.12 0 0
CUI: C1835875
Disease: Normocytic hypoplastic anemia
Normocytic hypoplastic anemia
1 0 1 0.12 0 0
CUI: C1835881
Disease: Fluctuating hepatomegaly
Fluctuating hepatomegaly
1 0 1 0.12 0 0
CUI: C1835882
Disease: Fluctuating splenomegaly
Fluctuating splenomegaly
1 0 1 0.12 0 0
Rhizomelic chondrodysplasia punctata, type 3
1 0 1 0.12 0 0
SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS
1 0 1 0.12 0 0
Rhizomelic chondrodysplasia punctata, type 2
1 0 1 0.12 0 0
Stippled calcification proximal humeral epiphyses
1 0 1 0.12 0 0
Calcific stippling of infantile cartilaginous skeleton
1 0 1 0.12 0 0
CUI: C1861213
Disease: Wide-cupped costochondral junctions
Wide-cupped costochondral junctions
1 0 1 0.12 0 0
CUI: C1863423
Disease: Lumbar kyphosis in infancy
Lumbar kyphosis in infancy
1 0 1 0.12 0 0
CUI: C1864852
Disease: CATSHL syndrome
CATSHL syndrome
1 0 1 0.12 0 0
CUI: C1864854
Disease: Broad femoral metaphyses
Broad femoral metaphyses
1 0 1 0.12 0 0