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: C0272350
Disease: Dysfibrinogenemia, Congenital
Dysfibrinogenemia, Congenital 		6 8 3 0.27 1 0.12
CUI: C2584774
Disease: Congenital hypofibrinogenemia
Congenital hypofibrinogenemia 		6 0 3 0.27 0 0
CUI: C3463916
Disease: Complement Factor I (C3 inactivator) deficiency
Complement Factor I (C3 inactivator) deficiency 		6 0 3 0.27 0 0
CUI: C0587043
Disease: Right ventricular thrombus
Right ventricular thrombus 		2 0 2 0.25 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		9 0 3 0.21 0 0
CUI: C0232943
Disease: Intermenstrual heavy bleeding
Intermenstrual heavy bleeding 		10 0 3 0.20 0 0
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		13 0 3 0.17 0 0
CUI: C0015499
Disease: Hereditary Factor V Deficiency
Hereditary Factor V Deficiency 		7 0 2 0.15 0 0
CUI: C0036413
Disease: Scleredema Adultorum
Scleredema Adultorum 		1 0 1 0.12 0 0
CUI: C0038557
Disease: Submandibular Gland Diseases
Submandibular Gland Diseases 		1 0 1 0.12 0 0
CUI: C0342861
Disease: Uroporphyrinogen decarboxylase deficiency
Uroporphyrinogen decarboxylase deficiency 		1 0 1 0.12 0 0
CUI: C0343263
Disease: Chondrolysis of articular cartilage
Chondrolysis of articular cartilage 		1 0 1 0.12 0 0
CUI: C0523633
Disease: Fibronectin measurement
Fibronectin measurement 		1 0 1 0.12 0 0
CUI: C0853856
Disease: Staphylococcal abscess
Staphylococcal abscess 		1 0 1 0.12 0 0
CUI: C1262010
Disease: Post lumbar puncture syndrome
Post lumbar puncture syndrome 		1 0 1 0.12 0 0
CUI: C1859970
Disease: Hypodysfibrinogenemia, Congenital
Hypodysfibrinogenemia, Congenital 		1 0 1 0.12 0 0
CUI: C1866075
Disease: GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder) 		1 0 1 0.12 0 0
CUI: C1867968
Disease: Porphyria Cutanea Tarda, Type I
Porphyria Cutanea Tarda, Type I 		1 0 1 0.12 0 0
CUI: C2931631
Disease: Chromosome 7, trisomy mosaic
Chromosome 7, trisomy mosaic 		1 0 1 0.12 0 0
CUI: C2931707
Disease: Chromosome 15, trisomy mosaicism
Chromosome 15, trisomy mosaicism 		1 0 1 0.12 0 0
CUI: C3179037
Disease: Developmental Coxa Vara
Developmental Coxa Vara 		1 0 1 0.12 0 0
CUI: C4016070
Disease: Fibrinogen dusart phenotype
Fibrinogen dusart phenotype 		1 0 1 0.12 0 0
CUI: C4016097
Disease: FIBRINOGEN MILANO XII, DIGENIC PHENOTYPE
FIBRINOGEN MILANO XII, DIGENIC PHENOTYPE 		1 0 1 0.12 0 0
CUI: C4025275
Disease: Generalized distal tubular acidosis
Generalized distal tubular acidosis 		1 0 1 0.12 0 0
CUI: C4025307
Disease: Hyperconvex vertebral body endplates
Hyperconvex vertebral body endplates 		1 0 1 0.12 0 0