Spherocytosis, Type 4 MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Spherocytosis, Type 4
Unique ID: C567208
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567208
Entry Term(s): Spherocytosis, Hereditary, 4
Registry Numbers: 0
Heading Mapped to: *Spherocytosis, Hereditary
Frequency: 1
Note: aka SPH4 or HS4; mutations in SLC4A1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Spherocytosis, Type 4 Preferred

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