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: C2676443
Disease: Proximal radio-ulnar synostosis
Proximal radio-ulnar synostosis 		5 0 2 0.25 0 0
CUI: C1854442
Disease: SPLIT-HAND/FOOT MALFORMATION 4
SPLIT-HAND/FOOT MALFORMATION 4 		6 0 2 0.22 0 0
CUI: C1863204
Disease: ADULT SYNDROME
ADULT SYNDROME 		6 0 2 0.22 0 0
CUI: C4021164
Disease: Bicoronal synostosis
Bicoronal synostosis 		6 1 2 0.22 1 3.0E-02
CUI: C4082168
Disease: Partial duplication of thumb phalanx
Partial duplication of thumb phalanx 		12 0 3 0.21 0 0
CUI: C0015338
Disease: Exstrophy
Exstrophy 		1 0 1 0.20 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 0.20 0 0
CUI: C0158667
Disease: Aplasia of Lacrimal and Salivary Glands
Aplasia of Lacrimal and Salivary Glands 		1 4 1 0.20 2 5.7E-02
CUI: C0241633
Disease: Vaginal dryness
Vaginal dryness 		1 0 1 0.20 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis 		1 0 1 0.20 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia 		1 0 1 0.20 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis 		1 0 1 0.20 0 0
CUI: C1300256
Disease: Thanatophoric dysplasia, type 1
Thanatophoric dysplasia, type 1 		1 4 1 0.20 2 5.7E-02
CUI: C1302999
Disease: Ankyloblepharon filiforme adnatum
Ankyloblepharon filiforme adnatum 		1 0 1 0.20 0 0
CUI: C1449718
Disease: Endocrine Breast Diseases
Endocrine Breast Diseases 		1 0 1 0.20 0 0
CUI: C1516419
Disease: Cervical Mesonephric Adenocarcinoma
Cervical Mesonephric Adenocarcinoma 		1 0 1 0.20 0 0
CUI: C1516974
Disease: Estrogen Receptor Status - Clinical Trial Eligibility Criteria
Estrogen Receptor Status - Clinical Trial Eligibility Criteria 		1 0 1 0.20 0 0
CUI: C1517658
Disease: Cervical Keratinizing Squamous Cell Carcinoma
Cervical Keratinizing Squamous Cell Carcinoma 		1 0 1 0.20 0 0
CUI: C1561989
Disease: Limbal stem cell deficiency
Limbal stem cell deficiency 		19 0 4 0.20 0 0
CUI: C1851152
Disease: SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS
SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS 		1 1 1 0.20 1 3.0E-02
CUI: C1851878
Disease: OROFACIAL CLEFT 8
OROFACIAL CLEFT 8 		1 0 1 0.20 0 0
CUI: C1851885
Disease: Progressive alopecia
Progressive alopecia 		1 0 1 0.20 0 0
CUI: C1852407
Disease: Prominent scrotal raphe
Prominent scrotal raphe 		1 0 1 0.20 0 0
CUI: C1852411
Disease: Preauricular skin furrow
Preauricular skin furrow 		1 0 1 0.20 0 0
CUI: C1858562
Disease: ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3 		1 14 1 0.20 1 2.2E-02