amelogenesis imperfecta, hypomaturation type, Iia3

Preferred Label : amelogenesis imperfecta, hypomaturation type, Iia3;

MeSH note : mutations in WDR72;

MeSH synonym : Ai2a3;

Origin ID

C567706;

UMLS CUI

C2750771;

Currated CISMeF NLP mapping
- Amelogenesis imperfecta, hypomaturation type, iia3 [OMIM Phenotype]
- amelogenesis imperfecta hypomaturation type 2A3 [DO Concept]
MeSH term(s) associated for indexing
- amelogenesis imperfecta [MeSH Descriptor]
Record concept(s)
- amelogenesis imperfecta, hypomaturation type, Iia3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Amelogenesis imperfecta, hypomaturation type, iia3 [OMIM Phenotype]
- amelogenesis imperfecta hypomaturation type 2A3 [DO Concept]