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: C0001145
Disease: Acne Keloid
Acne Keloid 		1 0 1 1.4E-02 0 0
CUI: C0012767
Disease: Tooth eruption disorder
Tooth eruption disorder 		1 0 1 1.4E-02 0 0
CUI: C0034882
Disease: Rectal Diseases
Rectal Diseases 		1 0 1 1.4E-02 0 0
CUI: C0040422
Disease: Tonsillar Neoplasms
Tonsillar Neoplasms 		1 0 1 1.4E-02 0 0
CUI: C0041971
Disease: Urethral Neoplasms
Urethral Neoplasms 		1 0 1 1.4E-02 0 0
CUI: C0151463
Disease: Abscess of breast
Abscess of breast 		1 0 1 1.4E-02 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 1.4E-02 0 0
CUI: C0152454
Disease: Symblepharon
Symblepharon 		1 0 1 1.4E-02 0 0
CUI: C0153618
Disease: Malignant tumor of renal pelvis
Malignant tumor of renal pelvis 		1 0 1 1.4E-02 0 0
CUI: C0155747
Disease: Aneurysm of splenic artery
Aneurysm of splenic artery 		1 0 1 1.4E-02 0 0
CUI: C0158651
Disease: Cleft lip, unilateral, complete
Cleft lip, unilateral, complete 		1 0 1 1.4E-02 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 1.4E-02 0 0
CUI: C0232874
Disease: Febrile proteinuria
Febrile proteinuria 		1 0 1 1.4E-02 0 0
CUI: C0234244
Disease: Tissue Pain
Tissue Pain 		1 0 1 1.4E-02 0 0
CUI: C0241060
Disease: Cyst of skin
Cyst of skin 		1 0 1 1.4E-02 0 0
CUI: C0243057
Disease: Stomatognathic System Abnormalities
Stomatognathic System Abnormalities 		1 0 1 1.4E-02 0 0
CUI: C0264081
Disease: Osteoarthropathy of fingers familial
Osteoarthropathy of fingers familial 		1 0 1 1.4E-02 0 0
CUI: C0265263
Disease: Femoral hypoplasia - unusual facies syndrome
Femoral hypoplasia - unusual facies syndrome 		1 0 1 1.4E-02 0 0
CUI: C0265280
Disease: Spondylometaphyseal dysplasia, Kozlowski type
Spondylometaphyseal dysplasia, Kozlowski type 		1 0 1 1.4E-02 0 0
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism 		1 0 1 1.4E-02 0 0
CUI: C0265363
Disease: Urethral obstruction sequence
Urethral obstruction sequence 		1 0 1 1.4E-02 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 1.4E-02 0 0
CUI: C0265669
Disease: Congenital dislocation of knee
Congenital dislocation of knee 		1 0 1 1.4E-02 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus 		1 0 1 1.4E-02 0 0
CUI: C0266501
Disease: Spina bifida of cervical region
Spina bifida of cervical region 		1 0 1 1.4E-02 0 0