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Hereditary alpha-tryptasemia syndrome MeSH Supplementary Concept Data 2025


MeSH Supplementary
Hereditary alpha-tryptasemia syndrome
Unique ID
C000715748
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C000715748
Entry Term(s)
Hereditary alpha-tryptasemia
Registry Numbers
0
Heading Mapped to
*Mast Cell Activation Syndrome
Frequency
6
Note
syndrome = extra copies of gene TPSAB1 with elevated ALPHA-TRYPTASE and several symptoms of mast cell activation syndrome; trait = extra copies of gene with elevated levels of alpha-tryptase but few or no symptoms; https://rarediseases.info.nih.gov/diseases/13193/hereditary-alpha-tryptasemia-syndrome
Date of Entry
2021/11/29
Revision Date
2021/11/24
Hereditary alpha-tryptasemia syndrome Preferred
Hereditary alpha-tryptasemia Broader
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