| Hereditary transthyretin related amyloidosis (disorder) | | Hereditary ATTR amyloidosis | | Hereditary transthyretin related amyloidosis
Hereditary TTR amyloidosis
Hereditary transthyretin amyloid polyneuropathy
Hereditary TTR amyloid polyneuropathy
ATTRv amyloidosis
Familial transthyretin-related amyloidosis
hATTR - hereditary transthyretin related amyloidosis
Familial TTR-related amyloidosis
| | A rare genetic systemic disease characterized by adult onset, progressive sensorimotor and autonomic neuropathy and infiltrative cardiomyopathy. Neurological involvement usually starts with sensory loss in the extremities and progresses with motor neuropathy. Cardiomyopathy presents with rhythm abnormalities and heart failure. The disease also frequently manifests with a range of additional clinical signs and symptoms due to associated ocular, renal, central nervous system and gastrointestinal involvement. |
| | Id | 1354544003 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | E85.1 | | Rule | TRUE | | Advice | ALWAYS E85.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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