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Catecholaminergic Polymorphic Ventricular Tachycardia 1

Disease ID: disease_node_19150

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Dbxref	ICD10CM:I42.8, ICD10CM:I47.2, MIM:604772
Subclassof	DOID_0060674
Data Source	DOID
Synonyms	CVPT1, arrhythmogenic right ventricular dysplasia 2
Doid Label	catecholaminergic polymorphic ventricular tachycardia 1
Doid Description	A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal domit inheritance and has_material_basis_in heterozygous mutation in the RYR2 gene on chromosome 1q43.
Has Symptom	SYMP_0000827
Disease Node Id	disease_node_19150
Doid Id	DOID_0060675
Label	Catecholaminergic Polymorphic Ventricular Tachycardia 1
Doid Alternate Ids	DOID_0110071

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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