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Hypomaturation amelogenesis imperfecta

Orpha number ORPHA100033
Synonym(s) Amelogenesis imperfecta type 2
Prevalence -
Inheritance Autosomal dominant
Autosomal recessive
X-linked recessive
Age of onset -
ICD-10
  • K00.5
ICD-O -
OMIM
UMLS
  • C0399372
MeSH
  • C536606
MedDRA -

Summary

This disease is described under Amelogenesis imperfecta


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