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Metadata
ID DOID:0110065
Name amelogenesis imperfecta type 1F
Definition An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the ameloblastin gene (AMBN) on chromosome 4q13.
https://www.ncbi.nlm.nih.gov/pubmed/24858907
Xrefs

ICD10CM:K00.5

OMIM:616270

Synonyms

AI1F [EXACT]

amelogenesis imperfecta hypoplastic type IF [EXACT]

amelogenesis imperfecta type IF [EXACT]

Parent Relationships

is_a amelogenesis imperfecta

is_a autosomal recessive disease

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