amelogenesis imperfecta, hypomaturation type, Iia1

Preferred Label : amelogenesis imperfecta, hypomaturation type, Iia1;

MeSH synonym : amelogenesis imperfecta, pigmented hypomaturation type, 1; Ai2a1;

Details

Origin ID

C567146;

UMLS CUI

C2673922;

Currated CISMeF NLP mapping
- Amelogenesis imperfecta, hypomaturation type, iia1 [OMIM Phenotype]
- amelogenesis imperfecta type 2A1 [DO Concept]
MeSH term(s) associated for indexing
- amelogenesis imperfecta [MeSH Descriptor]
Record concept(s)
- amelogenesis imperfecta, hypomaturation type, Iia1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Amelogenesis imperfecta, hypomaturation type, iia1 [OMIM Phenotype]
- amelogenesis imperfecta type 2A1 [DO Concept]

Keyword's position in hierarchy(ies) :

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