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: C0241633
Disease: Vaginal dryness
Vaginal dryness 		1 0 1 4.8E-02 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta 		1 0 1 4.8E-02 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula 		1 0 1 4.8E-02 0 0
CUI: C0344787
Disease: Complete atrioventricular septal defect
Complete atrioventricular septal defect 		1 0 1 4.8E-02 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia 		1 0 1 4.8E-02 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis 		1 0 1 4.8E-02 0 0
CUI: C0795812
Disease: Chromosome 4, trisomy 4q
Chromosome 4, trisomy 4q 		1 0 1 4.8E-02 0 0
CUI: C0795868
Disease: Chromosome 18, tetrasomy 18p
Chromosome 18, tetrasomy 18p 		1 0 1 4.8E-02 0 0
CUI: C0795939
Disease: AMINOPTERIN SYNDROME SINE AMINOPTERIN
AMINOPTERIN SYNDROME SINE AMINOPTERIN 		1 0 1 4.8E-02 0 0
CUI: C1302999
Disease: Ankyloblepharon filiforme adnatum
Ankyloblepharon filiforme adnatum 		1 0 1 4.8E-02 0 0
CUI: C1333502
Disease: extragonadal seminoma
extragonadal seminoma 		1 0 1 4.8E-02 0 0
CUI: C1449718
Disease: Endocrine Breast Diseases
Endocrine Breast Diseases 		1 0 1 4.8E-02 0 0
CUI: C1516419
Disease: Cervical Mesonephric Adenocarcinoma
Cervical Mesonephric Adenocarcinoma 		1 0 1 4.8E-02 0 0
CUI: C1516974
Disease: Estrogen Receptor Status - Clinical Trial Eligibility Criteria
Estrogen Receptor Status - Clinical Trial Eligibility Criteria 		1 0 1 4.8E-02 0 0
CUI: C1517658
Disease: Cervical Keratinizing Squamous Cell Carcinoma
Cervical Keratinizing Squamous Cell Carcinoma 		1 0 1 4.8E-02 0 0
CUI: C1841686
Disease: Absent hallux
Absent hallux 		1 0 1 4.8E-02 0 0
CUI: C1844529
Disease: Midclavicular aplasia
Midclavicular aplasia 		1 0 1 4.8E-02 0 0
CUI: C1851878
Disease: OROFACIAL CLEFT 8
OROFACIAL CLEFT 8 		1 0 1 4.8E-02 0 0
CUI: C1851885
Disease: Progressive alopecia
Progressive alopecia 		1 0 1 4.8E-02 0 0
CUI: C1852407
Disease: Prominent scrotal raphe
Prominent scrotal raphe 		1 0 1 4.8E-02 0 0
CUI: C1852411
Disease: Preauricular skin furrow
Preauricular skin furrow 		1 0 1 4.8E-02 0 0
CUI: C1855003
Disease: Bilateral postaxial polydactyly
Bilateral postaxial polydactyly 		1 0 1 4.8E-02 0 0
CUI: C1858562
Disease: ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3 		1 0 1 4.8E-02 0 0
CUI: C1862858
Disease: Red, cracking, peeling skin at birth
Red, cracking, peeling skin at birth 		1 0 1 4.8E-02 0 0
CUI: C1863392
Disease: Abnormal morphology of the limbic system
Abnormal morphology of the limbic system 		1 0 1 4.8E-02 0 0