Visualize Submit Comment
Metadata
ID DOID:0110063
Name amelogenesis imperfecta hypomaturation type 2A5
Definition An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the SLC24A4 gene on chromosome 14q32.
https://www.ncbi.nlm.nih.gov/pubmed/23375655
Xrefs

ICD10CM:K00.5

MIM:615887

Synonyms

AI2A5 [EXACT]

amelogenesis imperfecta hypomaturation type IIA5 [EXACT]

amelogenesis imperfecta type IIA5 [EXACT]

Parent Relationships

is_a amelogenesis imperfecta

is_a autosomal recessive disease

Add an item to the term tracker