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Nonsyndromic Aplasia Cutis Congenita

Disease ID: disease_node_20720

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Dbxref	MIM:107600
Subclassof	DOID_37
Data Source	DOID
Doid Label	nonsyndromic aplasia cutis congenita
Doid Description	A skin disease characterized by localized areas of missing skin that resemble ulcers or oopen wounds in new borns and that has_material_basis_in heterozygous mutation in the BMS1 gene on chromosome 10q11.
Disease Node Id	disease_node_20720
Doid Id	DOID_0080661
Label	Nonsyndromic Aplasia Cutis Congenita

Outgoing r'ship SUBCLASS_OF to/from Skin Diseases(ID:disease_node_6968) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Skin Diseases, Genetic(ID:disease_node_6970) (Disease)

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