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Ontology Browser

Amelogenesis Imperfecta Hypomaturation Type, 2A6 (DOID:9006208)
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Parent Terms Term With Siblings Child Terms
Amelogenesis Imperfecta Hypomaturation Type, 2A6 
Autosomal recessive amelogenesis imperfecta of the pigmented hypomaturation type characterized by slightly soft enamel of normal thickness that is hypomineralized and detaches easily from the dentin. (OMIM)

Exact Synonyms: AI2A6 ;   Amelogenesis Imperfecta, Hypomaturation Type, IIA6
Alternate IDs: RDO:9001336
Replaced By: DOID:0080960

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