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: C1852169
Disease: Periapical bone loss
Periapical bone loss 		2 0 2 0.40 0 0
CUI: C4023558
Disease: Dentinogenesis imperfecta limited to primary teeth
Dentinogenesis imperfecta limited to primary teeth 		2 0 2 0.40 0 0
CUI: C0205730
Disease: Hereditary Opalescent Dentin (disorder)
Hereditary Opalescent Dentin (disorder) 		1 0 1 0.20 0 0
CUI: C0809936
Disease: Branchio-skeleto-genital syndrome
Branchio-skeleto-genital syndrome 		1 0 1 0.20 0 0
CUI: C1854146
Disease: Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1
Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 		1 0 1 0.20 0 0
CUI: C1863870
Disease: Hypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss
Hypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss 		1 0 1 0.20 0 0
CUI: C3276551
Disease: DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH
DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH 		1 0 1 0.20 0 0
CUI: C4016014
Disease: DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 39, WITH DENTINOGENESIS IMPERFECTA 1
DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 39, WITH DENTINOGENESIS IMPERFECTA 1 		1 0 1 0.20 0 0
CUI: C4021299
Disease: Abnormality of dentin
Abnormality of dentin 		1 0 1 0.20 0 0
CUI: C4021828
Disease: Advanced pneumatization of the mastoid process
Advanced pneumatization of the mastoid process 		1 0 1 0.20 0 0
CUI: C4024197
Disease: Amelia involving the lower limbs
Amelia involving the lower limbs 		1 0 1 0.20 0 0
CUI: C4024199
Disease: Upper limb peromelia
Upper limb peromelia 		1 0 1 0.20 0 0
CUI: C4025057
Disease: Obliteration of the pulp chamber
Obliteration of the pulp chamber 		1 0 1 0.20 0 0
CUI: C4049050
Disease: Opalescent dentin
Opalescent dentin 		1 0 1 0.20 0 0
CUI: C4073208
Disease: Abnormality of the shape of the midface
Abnormality of the shape of the midface 		1 0 1 0.20 0 0
CUI: C4551670
Disease: Exodeviation
Exodeviation 		1 0 1 0.20 0 0
CUI: C0011430
Disease: Dentin Dysplasia
Dentin Dysplasia 		16 0 3 0.17 0 0
CUI: C0399380
Disease: Dentin dyspalsia, Shields type 2
Dentin dyspalsia, Shields type 2 		2 0 1 0.17 0 0
CUI: C1832560
Disease: RIPPLING MUSCLE DISEASE 2 (disorder)
RIPPLING MUSCLE DISEASE 2 (disorder) 		2 0 1 0.17 0 0
CUI: C3280443
Disease: MYOPATHY, DISTAL, TATEYAMA TYPE
MYOPATHY, DISTAL, TATEYAMA TYPE 		2 0 1 0.17 0 0
CUI: C4024661
Disease: Abnormality of the vertebral spinous processes
Abnormality of the vertebral spinous processes 		2 0 1 0.17 0 0
CUI: C0399378
Disease: Dentinogenesis imperfecta - Shield's type III (disorder)
Dentinogenesis imperfecta - Shield's type III (disorder) 		3 0 1 0.14 0 0
CUI: C1527284
Disease: Dental Pulp Stone
Dental Pulp Stone 		3 0 1 0.14 0 0
CUI: C1839965
Disease: Multiple impacted teeth
Multiple impacted teeth 		3 0 1 0.14 0 0
CUI: C1848869
Disease: Absent external genitalia
Absent external genitalia 		3 0 1 0.14 0 0