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: C0028878
Disease: Odontogenesis Imperfecta
Odontogenesis Imperfecta 		4 0 4 0.80 0 0
CUI: C0868847
Disease: Hereditary disturbances in tooth structure, not elsewhere classified in ICD10CM
Hereditary disturbances in tooth structure, not elsewhere classified in ICD10CM 		4 0 4 0.80 0 0
CUI: C0011430
Disease: Dentin Dysplasia
Dentin Dysplasia 		16 0 5 0.31 0 0
CUI: C0205730
Disease: Hereditary Opalescent Dentin (disorder)
Hereditary Opalescent Dentin (disorder) 		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: C2673923
Disease: Amelogenesis Imperfecta, Type Ic
Amelogenesis Imperfecta, Type Ic 		1 0 1 0.20 0 0
CUI: C2675858
Disease: Amelogenesis Imperfecta, Hypomaturation Type, Iia2
Amelogenesis Imperfecta, Hypomaturation Type, Iia2 		1 0 1 0.20 0 0
CUI: C2750771
Disease: Amelogenesis Imperfecta, Hypomaturation Type, Iia3
Amelogenesis Imperfecta, Hypomaturation Type, Iia3 		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: C4023540
Disease: Hypomature dental enamel
Hypomature dental enamel 		1 0 1 0.20 0 0
CUI: C4049050
Disease: Opalescent dentin
Opalescent dentin 		1 0 1 0.20 0 0
CUI: C0399372
Disease: Amelogenesis Imperfecta hypomaturation type
Amelogenesis Imperfecta hypomaturation type 		8 0 2 0.18 0 0
CUI: C0399380
Disease: Dentin dyspalsia, Shields type 2
Dentin dyspalsia, Shields type 2 		2 0 1 0.17 0 0
CUI: C1852169
Disease: Periapical bone loss
Periapical bone loss 		2 0 1 0.17 0 0
CUI: C1969038
Disease: RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder)
RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder) 		2 0 1 0.17 0 0
CUI: C4023558
Disease: Dentinogenesis imperfecta limited to primary teeth
Dentinogenesis imperfecta limited to primary teeth 		2 0 1 0.17 0 0
CUI: C0011436
Disease: Dentinogenesis Imperfecta
Dentinogenesis Imperfecta 		35 0 5 0.14 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: C1845053
Disease: Amelogenesis Imperfecta, Hypomaturation Type, with Snow-Capped Teeth
Amelogenesis Imperfecta, Hypomaturation Type, with Snow-Capped Teeth 		3 0 1 0.14 0 0
CUI: C2750327
Disease: Hearing loss, sensorineural (high frequency)
Hearing loss, sensorineural (high frequency) 		3 0 1 0.14 0 0
CUI: C2973527
Disease: Dentinogenesis imperfecta without osteogenesis imperfecta
Dentinogenesis imperfecta without osteogenesis imperfecta 		3 0 1 0.14 0 0
CUI: C0266060
Disease: Anterior open bite
Anterior open bite 		13 0 2 0.12 0 0
CUI: C0399379
Disease: Dentin dysplasia, type 1
Dentin dysplasia, type 1 		5 0 1 0.11 0 0
CUI: C0399368
Disease: Amelogenesis Imperfecta, Type IB
Amelogenesis Imperfecta, Type IB 		6 0 1 1.0E-01 0 0