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Metadata
ID DOID:0110062
Name amelogenesis imperfecta hypomaturation type 2A4
Definition An amelogenesis imperfecta caused by homozygous mutation in the C4ORF26 gene on chromosome 4q21.
https://www.ncbi.nlm.nih.gov/pubmed/22901946
Xrefs

ICD10CM:K00.5

MIM:614832

Synonyms

AI2A4 [EXACT]

amelogenesis imperfecta hypomaturation type IIA4 [EXACT]

amelogenesis imperfecta type IIA4 [EXACT]

Parent Relationships

is_a amelogenesis imperfecta

is_a autosomal recessive disease

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