Preferred Label : prealbumin;
Origin ID : F-62030;
UMLS CUI : C0032923;
Automatic exact mappings (from CISMeF team)
- Currated CISMeF NLP mapping
- Décrit
- SNOMED CT concept
- Semantic type(s)
- UMLS correspondences (same concept)
https://www.has-sante.fr/jcms/p_3638357/fr/wainzua-eplontersen-amylose-hereditaire-a-transthyretine-avec-polyneuropathie
2025
France
evaluation of the transparency committee
eplontersen
amylose
polyneuropathies
eplontersen
amyloidosis, hereditary, Transthyretin-Related
amyloidosis, nos
prealbumin
polyneuropathy, nos
amyloid deposition, nos
prealbumin
---
https://www.has-sante.fr/jcms/p_3351757/fr/neuropathie-amyloide-hereditaire-a-transthyretine-nah-ttr
2022
France
practice guideline
Neuropathy
chronic disease, nos
hereditary diseases
Handbook
prealbumin
hereditary disease, nos
amyloidosis, nos
amyloid neuropathies, familial
chronic disease
Hereditary disease
Chronic disease
prealbumin
Diseases
disorder of the peripheral nervous system, nos
amyloid neuropathies
---
