amelogenesis imperfecta
http://purl.obolibrary.org/obo/MONDO_0019507
Amelogenesis imperfecta (AI) represents a group of developmental conditions affecting the structure and clinical appearance of the enamel of all or nearly all the teeth in a more or less equal manner, and which may be associated with morphologic or biochemical changes elsewhere in the body. [ Orphanet:88661 ]
Term info
- ICD9:520.5 (MONDO:relatedTo)
- GARD:0005791 (MONDO:equivalentTo)
- MESH:D000567 (Orphanet:88661/e)
- Orphanet:88661 (MONDO:equivalentTo)
- DOID:2187 (MONDO:equivalentTo)
- CSP:0828-0533 (DOID:2187)
- OMIMPS:104500 (MONDO:equivalentTo)
- SCTID:78494001 (MONDO:equivalentTo)
gard_rare, ordo_disease, clingen
Amelogenesis imperfecta (AI) represents a group of developmental conditions affecting the structure and clinical appearance of the enamel of all or nearly all the teeth in a more or less equal manner, and which may be associated with morphologic or biochemical changes elsewhere in the body.
http://identifiers.org/snomedct/78494001, http://purl.obolibrary.org/obo/Orphanet_88661, https://omim.org/phenotypicSeries/PS104500, http://purl.obolibrary.org/obo/DOID_2187, http://identifiers.org/mesh/D000567
MONDO:0019507
https://rarediseases.info.nih.gov/diseases/5791/amelogenesis-imperfecta