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: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0 21 0 0 1 2.6E-03
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
1 0 1 6.1E-03 0 0
CUI: C0010273
Disease: Craniofacial Dysostosis
Craniofacial Dysostosis
1 0 1 6.1E-03 0 0
CUI: C0016063
Disease: Osteitis Fibrosa Disseminata
Osteitis Fibrosa Disseminata
1 0 1 6.1E-03 0 0
CUI: C0016065
Disease: Polyostotic fibrous dysplasia
Polyostotic fibrous dysplasia
1 0 1 6.1E-03 0 0
CUI: C0017097
Disease: Gardner Syndrome
Gardner Syndrome
1 0 1 6.1E-03 0 0
CUI: C0032580
Disease: Adenomatous Polyposis Coli
Adenomatous Polyposis Coli
1 0 1 6.1E-03 0 0
CUI: C0033835
Disease: Pseudopseudohypoparathyroidism
Pseudopseudohypoparathyroidism
1 0 1 6.1E-03 0 0
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea
1 0 1 6.1E-03 0 0
CUI: C0206724
Disease: Sex Cord-Stromal Tumor
Sex Cord-Stromal Tumor
1 0 1 6.1E-03 0 0
CUI: C0242292
Disease: McCune-Albright Syndrome
McCune-Albright Syndrome
1 0 1 6.1E-03 0 0
CUI: C0262401
Disease: Carcinoma of ampulla of Vater
Carcinoma of ampulla of Vater
1 0 1 6.1E-03 0 0
CUI: C0266357
Disease: Persistent umbilical sinus
Persistent umbilical sinus
1 0 1 6.1E-03 0 0
CUI: C0266445
Disease: Congenital atresia of vas deferens
Congenital atresia of vas deferens
1 0 1 6.1E-03 0 0
CUI: C0334041
Disease: Osteoma cutis
Osteoma cutis
1 0 1 6.1E-03 0 0
CUI: C0342684
Disease: Ocular albinism, type I
Ocular albinism, type I
1 0 1 6.1E-03 0 0
CUI: C0349661
Disease: Glial tumor of brain (disorder)
Glial tumor of brain (disorder)
1 0 1 6.1E-03 0 0
CUI: C0431693
Disease: Renal cysts and diabetes syndrome
Renal cysts and diabetes syndrome
1 0 1 6.1E-03 0 0
CUI: C0442774
Disease: Visual acuity, no light perception
Visual acuity, no light perception
1 0 1 6.1E-03 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis
1 0 1 6.1E-03 0 0
CUI: C0796121
Disease: Primrose syndrome
Primrose syndrome
1 0 1 6.1E-03 0 0
CUI: C1409412
Disease: Periostosis
Periostosis
1 0 1 6.1E-03 0 0
CUI: C1510455
Disease: Acrocephalosyndactylia
Acrocephalosyndactylia
1 0 1 6.1E-03 0 0
Estrogen Receptor Status - Clinical Trial Eligibility Criteria
1 0 1 6.1E-03 0 0
CUI: C1518693
Disease: Clear cell adenocarcinoma of ovary
Clear cell adenocarcinoma of ovary
1 0 1 6.1E-03 0 0