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: C4024210
Disease: Lester's sign
Lester's sign
1 0 1 0.17 0 0
CUI: C4024473
Disease: Radial deviation of the 4th finger
Radial deviation of the 4th finger
1 0 1 0.17 0 0
CUI: C4024674
Disease: Hypoplastic spinal processes
Hypoplastic spinal processes
1 0 1 0.17 0 0
CUI: C4025048
Disease: Elongated radius
Elongated radius
1 0 1 0.17 0 0
Thin proximal phalanges with broad epiphyses of the hand
1 0 1 0.17 0 0
CUI: C4025088
Disease: Broad metacarpal epiphyses
Broad metacarpal epiphyses
1 0 1 0.17 0 0
Abnormality of inferior oblique extraocular muscle
1 1 1 0.17 1 1.00
CUI: C4275033
Disease: Syndactyly type 1
Syndactyly type 1
1 0 1 0.17 0 0
BRACHYDACTYLY-SYNDACTYLY-OLIGODACTYLY SYNDROME
1 0 1 0.17 0 0
CUI: C0265312
Disease: Brachydactyly syndrome type E
Brachydactyly syndrome type E
2 0 1 0.14 0 0
CUI: C0403548
Disease: Salcedo syndrome
Salcedo syndrome
2 0 1 0.14 0 0
CUI: C0431928
Disease: Congenital overgrowth of lower limb
Congenital overgrowth of lower limb
2 2 1 0.14 1 0.50
CUI: C0432282
Disease: Dysplasia epiphysealis hemimelica
Dysplasia epiphysealis hemimelica
2 0 1 0.14 0 0
CUI: C1832590
Disease: Craniosynostosis, Philadelphia Type
Craniosynostosis, Philadelphia Type
2 0 1 0.14 0 0
CUI: C1834384
Disease: Glenoid fossa hypoplasia
Glenoid fossa hypoplasia
2 0 1 0.14 0 0
CUI: C1853137
Disease: BRACHYDACTYLY-SYNDACTYLY SYNDROME
BRACHYDACTYLY-SYNDACTYLY SYNDROME
2 0 1 0.14 0 0
CUI: C1855091
Disease: Short proximal phalanx of thumb
Short proximal phalanx of thumb
2 0 1 0.14 0 0
CUI: C1861328
Disease: Hypoplastic nasal septum
Hypoplastic nasal septum
2 0 1 0.14 0 0
CUI: C1861339
Disease: Absent distal phalanges
Absent distal phalanges
2 0 1 0.14 0 0
2nd-5th toe middle phalangeal hypoplasia
2 0 1 0.14 0 0
CUI: C1861388
Disease: Short 5th metacarpal
Short 5th metacarpal
10 0 2 0.14 0 0
CUI: C1864298
Disease: Fibular overgrowth
Fibular overgrowth
2 0 1 0.14 0 0
CUI: C1969652
Disease: BRACHYDACTYLY, TYPE B2 (disorder)
BRACHYDACTYLY, TYPE B2 (disorder)
2 0 1 0.14 0 0
CUI: C1970591
Disease: Abnormal pupillary light reflex
Abnormal pupillary light reflex
2 1 1 0.14 1 1.00
CUI: C4021537
Disease: Congenital conductive hearing loss
Congenital conductive hearing loss
2 0 1 0.14 0 0