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Amelogenesis Imperfecta Hypomaturation Type 2A3

Disease ID: disease_node_18114

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Dbxref	ICD10CM:K00.5, MIM:613211
Subclassof	DOID_0050737, DOID_2187
Data Source	DOID
Synonyms	AI2A3, amelogenesis imperfecta hypomaturation type IIA3, amelogenesis imperfecta type IIA3
Doid Label	amelogenesis imperfecta hypomaturation type 2A3
Doid Description	An amelogenesis imperfecta caused by homozygous mutation in the WDR72 gene.
Has Material Basis In	GENO_0000148
Disease Node Id	disease_node_18114
Doid Id	DOID_0110061
Label	Amelogenesis Imperfecta Hypomaturation Type 2A3

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

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