MeSH Browser

MeSH Heading: Amelogenesis Imperfecta
Tree Number(s): C07.650.800.295.250; C07.793.700.295.250; C16.131.850.800.295.250
Unique ID: D000567
RDF Unique Identifier: http://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.
Entry Term(s): Congenital Enamel Hypoplasia
Public MeSH Note: 65
History Note: 65
Date Established: 1965/01/01
Date of Entry: 1999/01/01
Revision Date: 2022/05/23

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Amelogenesis Imperfecta MeSH Descriptor Data 2024