| Descriptor English: | Amelogenesis Imperfecta | ||||
| Descriptor Spanish: |
Amelogénesis Imperfecta
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| Descriptor Portuguese: | Amelogênese Imperfeita | ||||
| Descriptor French: | Amélogenèse imparfaite | ||||
| Entry term(s): |
Congenital Enamel Hypoplasia |
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| Tree number(s): |
C07.650.800.295.250 C07.793.700.295.250 C16.131.850.800.295.250 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000567 | ||||
| Scope note: | A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 65 |
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| History Note: | 65 |
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| DeCS ID: | 569 | ||||
| Unique ID: | D000567 | ||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
| Date Established: | 1965/01/01 | ||||
| Date of Entry: | 1999/01/01 | ||||
| Revision Date: | 2013/07/08 |
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Amelogenesis Imperfecta
- Preferred
| Concept UI |
M0000886 |
| Scope note | A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION. |
| Preferred term | Amelogenesis Imperfecta |
| Entry term(s) |
Congenital Enamel Hypoplasia |
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