Dentinogenesis imperfecta

Symptom Information:

Symptom ID: HPO:0000703
Synonyms:
Dentinogenesis imperfecta [OMIM:Dentinogenesis imperfecta]
Dentinogenesis imperfecta (both primary and secondary teeth) [OMIM:Dentinogenesis imperfecta (both primary and secondary teeth)]
Dentinogenesis imperfecta (in one family) [OMIM:Dentinogenesis imperfecta (in one family)]
Dentinogenesis imperfecta (rare) [OMIM:Dentinogenesis imperfecta (rare)]
Dentinogenesis imperfecta [MedDRA:10054013]
Quality:
Cross references:
OMIM: "Dentinogenesis imperfecta" [OMIM:Dentinogenesis imperfecta]
OMIM: "Dentinogenesis imperfecta (both primary and secondary teeth)" [OMIM:Dentinogenesis imperfecta (both primary and secondary teeth)]
OMIM: "Dentinogenesis imperfecta (in one family)" [OMIM:Dentinogenesis imperfecta (in one family)]
OMIM: "Dentinogenesis imperfecta (rare)" [OMIM:Dentinogenesis imperfecta (rare)]
Is a (Direct Parents):
HPO         Abnormality of dentin
MedDRA Dental disorders congenital
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the mouth(HPO:0000153)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of the teeth(HPO:0000164)
                         Abnormality of dental structure(HPO:0011061)
                            Abnormality of dentin(HPO:0010299)
                               Dentinogenesis imperfecta(HPO:0000703)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Gastrointestinal tract disorders congenital(MedDRA:10018018)
       Dental disorders congenital(MedDRA:10044036)
          Dentinogenesis imperfecta(HPO:0000703)
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

BRITTLE CORNEA SYNDROME 1 (OMIM:229200)
Brittle cornea syndrome (Orphanet:90354)
DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1 (OMIM:605594)
DENTINOGENESIS IMPERFECTA 1 (OMIM:125490)
Dentinogenesis imperfecta type 2 (Orphanet:166260)
Dentinogenesis imperfecta type 3 (Orphanet:166265)
Goldblatt syndrome (Orphanet:166272)
OSTEOGENESIS IMPERFECTA, TYPE I (OMIM:166200)
OSTEOGENESIS IMPERFECTA, TYPE III (OMIM:259420)
OSTEOGENESIS IMPERFECTA, TYPE IV (OMIM:166220)
OSTEOGENESIS IMPERFECTA, TYPE IX (OMIM:259440)
OSTEOGENESIS IMPERFECTA, TYPE X (OMIM:613848)
OSTEOGENESIS IMPERFECTA, TYPE XI (OMIM:610968)
Osteogenesis imperfecta type 1 (Orphanet:216796)
Osteogenesis imperfecta type 3 (Orphanet:216812)
Osteogenesis imperfecta type 4 (Orphanet:216820)
Osteogenesis imperfecta type 5 (Orphanet:216828)
Suarez-Stickler syndrome (Orphanet:166277)