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: C1516974
Disease: Estrogen Receptor Status - Clinical Trial Eligibility Criteria
Estrogen Receptor Status - Clinical Trial Eligibility Criteria 		1 0 1 0.14 0 0
CUI: C1517658
Disease: Cervical Keratinizing Squamous Cell Carcinoma
Cervical Keratinizing Squamous Cell Carcinoma 		1 0 1 0.14 0 0
CUI: C1517894
Disease: Lipid-Rich Breast Carcinoma
Lipid-Rich Breast Carcinoma 		1 0 1 0.14 0 0
CUI: C1563119
Disease: Hormone receptor positive tumor
Hormone receptor positive tumor 		1 0 1 0.14 0 0
CUI: C1832273
Disease: Ribbing disease
Ribbing disease 		1 0 1 0.14 0 0
CUI: C1836723
Disease: Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum
Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum 		1 0 1 0.14 0 0
CUI: C1851612
Disease: Narrowing of medullary canal
Narrowing of medullary canal 		1 0 1 0.14 0 0
CUI: C1852407
Disease: Prominent scrotal raphe
Prominent scrotal raphe 		1 0 1 0.14 0 0
CUI: C1852411
Disease: Preauricular skin furrow
Preauricular skin furrow 		1 0 1 0.14 0 0
CUI: C1863392
Disease: Abnormal morphology of the limbic system
Abnormal morphology of the limbic system 		1 0 1 0.14 0 0
CUI: C1863395
Disease: Acrobrachycephaly
Acrobrachycephaly 		1 0 1 0.14 0 0
CUI: C1863403
Disease: Broad distal hallux
Broad distal hallux 		1 0 1 0.14 0 0
CUI: C1865070
Disease: SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION
SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION 		1 0 1 0.14 0 0
CUI: C1867563
Disease: CRANIOSYNOSTOSIS, NONCLASSIFIABLE AUTOSOMAL DOMINANT
CRANIOSYNOSTOSIS, NONCLASSIFIABLE AUTOSOMAL DOMINANT 		1 0 1 0.14 0 0
CUI: C1867564
Disease: SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY
SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY 		1 0 1 0.14 0 0
CUI: C2063886
Disease: Esophageal Adenosquamous Carcinoma
Esophageal Adenosquamous Carcinoma 		1 0 1 0.14 0 0
CUI: C2126063
Disease: Exophthalmos, bilateral
Exophthalmos, bilateral 		1 0 1 0.14 0 0
CUI: C2242653
Disease: Thyroid fibrosis
Thyroid fibrosis 		1 0 1 0.14 0 0
CUI: C2717859
Disease: Peritoneal Sclerosis
Peritoneal Sclerosis 		1 0 1 0.14 0 0
CUI: C2930879
Disease: Cerebellar degeneration, subacute
Cerebellar degeneration, subacute 		1 0 1 0.14 0 0
CUI: C2931899
Disease: Papillary renal cell carcinoma, familial
Papillary renal cell carcinoma, familial 		1 0 1 0.14 0 0
CUI: C3267076
Disease: Familial scaphocephaly syndrome
Familial scaphocephaly syndrome 		1 0 1 0.14 0 0
CUI: C3463918
Disease: EMBRYONAL CELL CARCINOMA
EMBRYONAL CELL CARCINOMA 		1 0 1 0.14 0 0
CUI: C3544328
Disease: Prostatic fibrosis
Prostatic fibrosis 		1 0 1 0.14 0 0
CUI: C3552414
Disease: Deviation of the thumb
Deviation of the thumb 		1 0 1 0.14 0 0