amelogenesis imperfecta, type III

Preferred Label : amelogenesis imperfecta, type III;

MeSH synonym : amelogenesis imperfecta, hypomineralization type; amelogenesis imperfecta, hypocalcification type, autosomal dominant; ADHCAI;

Is substance : O;

Details

Origin ID

C562880;

UMLS CUI

C0399376;

Automatic exact mappings (from CISMeF team)
- amelogenesis imperfecta type 3A [DO Concept]
CISMeF manual mappings
- Hypocalcified amelogenesis imperfecta [ORDO Disease]
DO Cross reference
- amelogenesis imperfecta type 3 [DO Concept]
MeSH term(s) associated for indexing
- amelogenesis imperfecta [MeSH Descriptor]
Record concept(s)
- amelogenesis imperfecta, type III [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Amelogenesis imperfecta, hypocalcification type (disorder) [SNOMED CT concept]
- Amelogenesis imperfecta, type iiia [OMIM Phenotype]
- Hypocalcified amelogenesis imperfecta [ORDO Disease]
- amelogenesis imperfecta type 3 [DO Concept]
- amelogenesis imperfecta type III [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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