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Amelogenesis Imperfecta Hypomaturation Type 2A5

Disease ID: disease_node_18112

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Dbxref	ICD10CM:K00.5, MIM:615887
Subclassof	DOID_0050737, DOID_2187
Data Source	DOID
Synonyms	AI2A5, amelogenesis imperfecta hypomaturation type IIA5, amelogenesis imperfecta type IIA5
Doid Label	amelogenesis imperfecta hypomaturation type 2A5
Doid Description	An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the SLC24A4 gene on chromosome 14q32.
Has Material Basis In	GENO_0000148
Disease Node Id	disease_node_18112
Doid Id	DOID_0110063
Label	Amelogenesis Imperfecta Hypomaturation Type 2A5

Outgoing r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta(ID:disease_node_1139) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)

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