Dentinogenesis imperfecta
Symptom Information:
Symptom ID: | HPO:0000703 | |||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |