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| Term | atrial standstill 2 | ID (Ontology) | DOID:0080663 (Human Disease) |
| Definition | A heart conduction disease that is characterized by a transient or permanent absence of electrical and mechanical atrial activity and has_material_basis_in homozygous mutation in the NPPA gene on chromosome 1p36. | ||
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autosomal genetic disease |__autosomal recessive disease__ heart disease | |__heart conduction disease_____| atrial standstill 2 |
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| Is a |
autosomal recessive disease heart conduction disease |
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External Crossreferences & Linkouts
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| MIM:615745 | |||