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Catecholaminergic Polymorphic Ventricular Tachycardia 2

Disease ID: disease_node_19149

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Dbxref	ICD10CM:I47.2, MIM:611938
Subclassof	DOID_0060674
Data Source	DOID
Synonyms	CVPT2
Doid Label	catecholaminergic polymorphic ventricular tachycardia 2
Doid Description	A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal recessive inheritance and has_material_basis_in homozygous or compound heterozygous mutation in the CASQ2 gene on chromosome 1p13.
Has Symptom	SYMP_0000827
Disease Node Id	disease_node_19149
Doid Id	DOID_0060676
Label	Catecholaminergic Polymorphic Ventricular Tachycardia 2

Outgoing r'ship HAS_SYMPTOM to/from Ventricular Tachycardia(ID:disease_node_21137) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Catecholaminergic Polymorphic Ventricular Tachycardia(ID:disease_node_19145) (Disease)

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