amelogenesis imperfecta, hypomaturation type, Iia2

Preferred Label : amelogenesis imperfecta, hypomaturation type, Iia2;

MeSH synonym : Ai2a2; amelogenesis imperfecta, pigmented hypomaturation type, 2;

Details

Origin ID

C567279;

UMLS CUI

C2675858;

Currated CISMeF NLP mapping
- Amelogenesis imperfecta, hypomaturation type, iia2 [OMIM Phenotype]
- amelogenesis imperfecta hypomaturation type 2A2 [DO Concept]
MeSH term(s) associated for indexing
- amelogenesis imperfecta [MeSH Descriptor]
Record concept(s)
- amelogenesis imperfecta, hypomaturation type, Iia2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Amelogenesis imperfecta, hypomaturation type, iia2 [OMIM Phenotype]
- amelogenesis imperfecta hypomaturation type 2A2 [DO Concept]

Keyword's position in hierarchy(ies) :

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