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: C0574785
Disease: Lower Urinary Tract Symptoms
Lower Urinary Tract Symptoms 		77 30 7 7.4E-02 7 5.9E-02
CUI: C0034902
Disease: Pure Red-Cell Aplasia
Pure Red-Cell Aplasia 		49 0 3 4.2E-02 0 0
CUI: C0033579
Disease: Prostate nodule
Prostate nodule 		1 0 1 4.0E-02 0 0
CUI: C0238152
Disease: Cardiac Sarcoma
Cardiac Sarcoma 		1 0 1 4.0E-02 0 0
CUI: C0240812
Disease: Prostatic pain
Prostatic pain 		1 0 1 4.0E-02 0 0
CUI: C0266445
Disease: Congenital atresia of vas deferens
Congenital atresia of vas deferens 		1 0 1 4.0E-02 0 0
CUI: C0278834
Disease: Stage I Prostate Carcinoma
Stage I Prostate Carcinoma 		1 0 1 4.0E-02 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia 		1 0 1 4.0E-02 0 0
CUI: C0521663
Disease: Paraparesis, Chronic Progressive
Paraparesis, Chronic Progressive 		1 0 1 4.0E-02 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis 		1 0 1 4.0E-02 0 0
CUI: C1282799
Disease: Penile swelling
Penile swelling 		1 0 1 4.0E-02 0 0
CUI: C1335511
Disease: Prostate Leiomyosarcoma
Prostate Leiomyosarcoma 		1 0 1 4.0E-02 0 0
CUI: C1516419
Disease: Cervical Mesonephric Adenocarcinoma
Cervical Mesonephric Adenocarcinoma 		1 0 1 4.0E-02 0 0
CUI: C1516974
Disease: Estrogen Receptor Status - Clinical Trial Eligibility Criteria
Estrogen Receptor Status - Clinical Trial Eligibility Criteria 		1 0 1 4.0E-02 0 0
CUI: C1517658
Disease: Cervical Keratinizing Squamous Cell Carcinoma
Cervical Keratinizing Squamous Cell Carcinoma 		1 0 1 4.0E-02 0 0
CUI: C1519233
Disease: Seminal Vesicle Adenocarcinoma
Seminal Vesicle Adenocarcinoma 		1 0 1 4.0E-02 0 0
CUI: C1567427
Disease: Bilateral Multicystic Dysplastic Kidneys
Bilateral Multicystic Dysplastic Kidneys 		1 0 1 4.0E-02 0 0
CUI: C1852407
Disease: Prominent scrotal raphe
Prominent scrotal raphe 		1 0 1 4.0E-02 0 0
CUI: C1852411
Disease: Preauricular skin furrow
Preauricular skin furrow 		1 0 1 4.0E-02 0 0
CUI: C1863392
Disease: Abnormal morphology of the limbic system
Abnormal morphology of the limbic system 		1 0 1 4.0E-02 0 0
CUI: C1863395
Disease: Acrobrachycephaly
Acrobrachycephaly 		1 0 1 4.0E-02 0 0
CUI: C1863403
Disease: Broad distal hallux
Broad distal hallux 		1 0 1 4.0E-02 0 0
CUI: C1865070
Disease: SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION
SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION 		1 0 1 4.0E-02 0 0
CUI: C1867563
Disease: CRANIOSYNOSTOSIS, NONCLASSIFIABLE AUTOSOMAL DOMINANT
CRANIOSYNOSTOSIS, NONCLASSIFIABLE AUTOSOMAL DOMINANT 		1 0 1 4.0E-02 0 0
CUI: C1867564
Disease: SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY
SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY 		1 0 1 4.0E-02 0 0