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: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta
1 0 1 5.9E-02 0 0
CUI: C0266501
Disease: Spina bifida of cervical region
Spina bifida of cervical region
1 0 1 5.9E-02 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula
1 0 1 5.9E-02 0 0
CUI: C0341790
Disease: Neoplasm of scrotum
Neoplasm of scrotum
1 0 1 5.9E-02 0 0
CUI: C0432149
Disease: Lumbar hemivertebra
Lumbar hemivertebra
1 0 1 5.9E-02 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia
1 0 1 5.9E-02 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis
1 0 1 5.9E-02 0 0
Acromegaloid facial appearance syndrome
1 0 1 5.9E-02 0 0
CUI: C0878515
Disease: Internal hydrocephalus
Internal hydrocephalus
1 0 1 5.9E-02 0 0
CUI: C1300267
Disease: Brachydactyly syndrome type B
Brachydactyly syndrome type B
1 0 1 5.9E-02 0 0
CUI: C1327918
Disease: Oculootoradial syndrome
Oculootoradial syndrome
1 0 1 5.9E-02 0 0
CUI: C1333286
Disease: Diencephalic Neoplasm
Diencephalic Neoplasm
1 0 1 5.9E-02 0 0
CUI: C1333859
Disease: Grade 2 Colon Adenocarcinoma
Grade 2 Colon Adenocarcinoma
1 0 1 5.9E-02 0 0
CUI: C1516419
Disease: Cervical Mesonephric Adenocarcinoma
Cervical Mesonephric Adenocarcinoma
1 0 1 5.9E-02 0 0
Estrogen Receptor Status - Clinical Trial Eligibility Criteria
1 0 1 5.9E-02 0 0
Cervical Keratinizing Squamous Cell Carcinoma
1 0 1 5.9E-02 0 0
CUI: C1837839
Disease: CARDIOMYOPATHY, DILATED, 1O
CARDIOMYOPATHY, DILATED, 1O
1 0 1 5.9E-02 0 0
CUI: C1840086
Disease: Pectoralis major hypoplasia
Pectoralis major hypoplasia
1 0 1 5.9E-02 0 0
CUI: C1841686
Disease: Absent hallux
Absent hallux
1 0 1 5.9E-02 0 0
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2
1 0 1 5.9E-02 0 0
CUI: C1844722
Disease: Unilateral breast hypoplasia
Unilateral breast hypoplasia
1 0 1 5.9E-02 0 0
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
1 0 1 5.9E-02 0 0
CUI: C1846478
Disease: Upper limb muscle hypoplasia
Upper limb muscle hypoplasia
1 0 1 5.9E-02 0 0
CUI: C1852407
Disease: Prominent scrotal raphe
Prominent scrotal raphe
1 0 1 5.9E-02 0 0
CUI: C1852411
Disease: Preauricular skin furrow
Preauricular skin furrow
1 0 1 5.9E-02 0 0