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: C2981132
Disease: Shell teeth
Shell teeth 		5 0 5 0.31 0 0
CUI: C0011436
Disease: Dentinogenesis Imperfecta
Dentinogenesis Imperfecta 		35 0 11 0.28 0 0
CUI: C0028878
Disease: Odontogenesis Imperfecta
Odontogenesis Imperfecta 		4 0 4 0.25 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 0.25 0 0
CUI: C0399378
Disease: Dentinogenesis imperfecta - Shield's type III (disorder)
Dentinogenesis imperfecta - Shield's type III (disorder) 		3 0 3 0.19 0 0
CUI: C0399379
Disease: Dentin dysplasia, type 1
Dentin dysplasia, type 1 		5 0 3 0.17 0 0
CUI: C2973527
Disease: Dentinogenesis imperfecta without osteogenesis imperfecta
Dentinogenesis imperfecta without osteogenesis imperfecta 		3 0 2 0.12 0 0
CUI: C0027661
Disease: Neoplasms, Hormone-Dependent
Neoplasms, Hormone-Dependent 		4 0 2 0.11 0 0
CUI: C0399372
Disease: Amelogenesis Imperfecta hypomaturation type
Amelogenesis Imperfecta hypomaturation type 		8 0 2 9.1E-02 0 0
CUI: C2930618
Disease: Intersex Conditions
Intersex Conditions 		9 0 2 8.7E-02 0 0
CUI: C1334011
Disease: High Grade Cervical Intraepithelial Neoplasia
High Grade Cervical Intraepithelial Neoplasia 		51 0 5 8.1E-02 0 0
CUI: C0266060
Disease: Anterior open bite
Anterior open bite 		13 0 2 7.4E-02 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		61 0 5 6.9E-02 0 0
CUI: C0033804
Disease: Pseudohermaphroditism
Pseudohermaphroditism 		16 0 2 6.7E-02 0 0
CUI: C1704330
Disease: Dental Diseases
Dental Diseases 		16 0 2 6.7E-02 0 0
CUI: C0027821
Disease: Neurocirculatory Asthenia
Neurocirculatory Asthenia 		1 0 1 6.2E-02 0 0
CUI: C0029630
Disease: Other heart block
Other heart block 		1 0 1 6.2E-02 0 0
CUI: C0205730
Disease: Hereditary Opalescent Dentin (disorder)
Hereditary Opalescent Dentin (disorder) 		1 0 1 6.2E-02 0 0
CUI: C0220743
Disease: Childhood hypophosphatasia (disorder)
Childhood hypophosphatasia (disorder) 		1 0 1 6.2E-02 0 0
CUI: C0232058
Disease: Apnea in the newborn
Apnea in the newborn 		1 0 1 6.2E-02 0 0
CUI: C1332951
Disease: Childhood Brain Stem Neoplasm
Childhood Brain Stem Neoplasm 		1 0 1 6.2E-02 0 0
CUI: C1840322
Disease: ODONTOHYPOPHOSPHATASIA (disorder)
ODONTOHYPOPHOSPHATASIA (disorder) 		1 0 1 6.2E-02 0 0
CUI: C1851129
Disease: Progressive cervical vertebral spine fusion
Progressive cervical vertebral spine fusion 		1 0 1 6.2E-02 0 0
CUI: C1854146
Disease: Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1
Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 		1 0 1 6.2E-02 0 0
CUI: C1855815
Disease: Skin dimple over apex of long bone angulation
Skin dimple over apex of long bone angulation 		1 0 1 6.2E-02 0 0