Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Macrodontia of permanent maxillary central incisor
8 1 1 1.0E-01 1 2.2E-02
CUI: C4022908
Disease: Cerebral white matter hypoplasia
Cerebral white matter hypoplasia
8 0 1 1.0E-01 0 0
CUI: C1303003
Disease: Epicanthus inversus
Epicanthus inversus
9 0 1 9.1E-02 0 0
Prostatic Neoplasms, Castration-Resistant
9 0 1 9.1E-02 0 0
CUI: C3830518
Disease: Diabetic embryopathy
Diabetic embryopathy
9 0 1 9.1E-02 0 0
CUI: C0158779
Disease: Cervical rib
Cervical rib
11 0 1 7.7E-02 0 0
CUI: C0332915
Disease: Congenital failure of fusion
Congenital failure of fusion
11 0 1 7.7E-02 0 0
CUI: C0749420
Disease: Thyroid Agenesis
Thyroid Agenesis
11 0 1 7.7E-02 0 0
CUI: C1850629
Disease: Exaggerated cupid's bow
Exaggerated cupid's bow
11 6 1 7.7E-02 1 2.0E-02
CUI: C1856121
Disease: Broad eyebrow
Broad eyebrow
11 4 1 7.7E-02 1 2.0E-02
CUI: C0266036
Disease: Macrodontia
Macrodontia
12 0 1 7.1E-02 0 0
CUI: C0302845
Disease: MCV - raised
MCV - raised
12 0 1 7.1E-02 0 0
Prostatic Cancer, Castration-Resistant
12 0 1 7.1E-02 0 0
CUI: C0151516
Disease: Thyroid Hypoplasia
Thyroid Hypoplasia
14 0 1 6.2E-02 0 0
CUI: C1859447
Disease: Hypoplastic ischia
Hypoplastic ischia
14 0 1 6.2E-02 0 0
CUI: C4023721
Disease: Abnormal hair pattern
Abnormal hair pattern
15 0 1 5.9E-02 0 0
CUI: C1835807
Disease: Prominent fingertip pads
Prominent fingertip pads
16 8 1 5.6E-02 1 1.9E-02
CUI: C1861218
Disease: Hypoplastic ilia
Hypoplastic ilia
16 0 1 5.6E-02 0 0
CUI: C4023385
Disease: Aplasia of the semicircular canal
Aplasia of the semicircular canal
16 0 1 5.6E-02 0 0
CUI: C0431664
Disease: Unilateral Cryptorchidism
Unilateral Cryptorchidism
17 5 1 5.3E-02 1 2.0E-02
CUI: C0796004
Disease: Kabuki make-up syndrome
Kabuki make-up syndrome
37 0 2 5.3E-02 0 0
CUI: C1861921
Disease: Cutaneous syndactyly
Cutaneous syndactyly
17 0 1 5.3E-02 0 0
CUI: C1868578
Disease: Patellar aplasia
Patellar aplasia
17 0 1 5.3E-02 0 0
CUI: C4021395
Disease: Abnormality of the antihelix
Abnormality of the antihelix
17 0 1 5.3E-02 0 0
CUI: C1954751
Disease: Microdeletion syndromes
Microdeletion syndromes
18 0 1 5.0E-02 0 0