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Congenital Nonspherocytic Hemolytic Anemia 4

Disease ID: disease_node_15266

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Dbxref	MIM:613470
Subclassof	DOID_2861, DOID_0050737
Data Source	DOID
Doid Label	congenital nonspherocytic hemolytic anemia 4
Doid Description	A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the PHI gene (GPI) on chromosome 19q13.
Has Material Basis In	GENO_0000148
Disease Node Id	disease_node_15266
Doid Id	DOID_0051005
Label	Congenital Nonspherocytic Hemolytic Anemia 4

Outgoing r'ship SUBCLASS_OF to/from Anemia, Hemolytic, Congenital Nonspherocytic(ID:disease_node_1189) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)

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