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: C1332042
Disease: AIDS-Related Diffuse Large B-cell Lymphoma
AIDS-Related Diffuse Large B-cell Lymphoma 		1 0 1 0.11 0 0
CUI: C1332913
Disease: Cervical Endometrioid Adenocarcinoma
Cervical Endometrioid Adenocarcinoma 		1 0 1 0.11 0 0
CUI: C1334664
Disease: Mediastinal Lymphangioma
Mediastinal Lymphangioma 		1 0 1 0.11 0 0
CUI: C1334695
Disease: Meningeal Gliomatosis
Meningeal Gliomatosis 		1 0 1 0.11 0 0
CUI: C1335389
Disease: Lipomatosis of Nerve
Lipomatosis of Nerve 		1 0 1 0.11 0 0
CUI: C1394320
Disease: Endometrial Cyst
Endometrial Cyst 		1 0 1 0.11 0 0
CUI: C1516419
Disease: Cervical Mesonephric Adenocarcinoma
Cervical Mesonephric Adenocarcinoma 		1 0 1 0.11 0 0
CUI: C1516974
Disease: Estrogen Receptor Status - Clinical Trial Eligibility Criteria
Estrogen Receptor Status - Clinical Trial Eligibility Criteria 		1 0 1 0.11 0 0
CUI: C1517658
Disease: Cervical Keratinizing Squamous Cell Carcinoma
Cervical Keratinizing Squamous Cell Carcinoma 		1 0 1 0.11 0 0
CUI: C1835047
Disease: MELANOMA, CUTANEOUS MALIGNANT, 1
MELANOMA, CUTANEOUS MALIGNANT, 1 		1 0 1 0.11 0 0
CUI: C1852407
Disease: Prominent scrotal raphe
Prominent scrotal raphe 		1 0 1 0.11 0 0
CUI: C1852411
Disease: Preauricular skin furrow
Preauricular skin furrow 		1 0 1 0.11 0 0
CUI: C1863392
Disease: Abnormal morphology of the limbic system
Abnormal morphology of the limbic system 		1 0 1 0.11 0 0
CUI: C1863395
Disease: Acrobrachycephaly
Acrobrachycephaly 		1 0 1 0.11 0 0
CUI: C1863403
Disease: Broad distal hallux
Broad distal hallux 		1 0 1 0.11 0 0
CUI: C1864730
Disease: Polyposis Syndrome, Hereditary Mixed, 2
Polyposis Syndrome, Hereditary Mixed, 2 		1 0 1 0.11 0 0
CUI: C1865070
Disease: SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION
SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION 		1 0 1 0.11 0 0
CUI: C1867563
Disease: CRANIOSYNOSTOSIS, NONCLASSIFIABLE AUTOSOMAL DOMINANT
CRANIOSYNOSTOSIS, NONCLASSIFIABLE AUTOSOMAL DOMINANT 		1 0 1 0.11 0 0
CUI: C1867564
Disease: SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY
SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY 		1 0 1 0.11 0 0
CUI: C1868007
Disease: Precocious puberty with Sertoli cell tumor
Precocious puberty with Sertoli cell tumor 		1 0 1 0.11 0 0
CUI: C1963768
Disease: Glycogenic acanthosis
Glycogenic acanthosis 		1 0 1 0.11 0 0
CUI: C1963822
Disease: Mucosal pigmentation
Mucosal pigmentation 		1 0 1 0.11 0 0
CUI: C2126063
Disease: Exophthalmos, bilateral
Exophthalmos, bilateral 		1 0 1 0.11 0 0
CUI: C2677102
Disease: Chromosome 10q23 Deletion Syndrome
Chromosome 10q23 Deletion Syndrome 		1 0 1 0.11 0 0
CUI: C2751313
Disease: CLAPO Syndrome
CLAPO Syndrome 		1 0 1 0.11 0 0