WormBase Tree Display for DO_term: DOID:0110646
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DOID:0110646 | Name | long QT syndrome 3 | |||
---|---|---|---|---|---|
Status | Valid | ||||
Definition | A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2. | ||||
Synonym | Exact | LQT3 | |||
Parent | Is_a | DOID:2843 | |||
DOID:0050736 | |||||
DOID:0080578 | |||||
DB_info | Database | OMIM | disease | 603830 |