Spherocytosis, Type 5 MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Spherocytosis, Type 5
Unique ID: C567202
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567202
Entry Term(s): Spherocytosis, Hereditary, 5
Registry Number: 0
Heading Mapped to: *Spherocytosis, Hereditary
Frequency: 0
Note: aka SPH5 or HS5; mutations in EPB42
Date of Entry: 2012/11/05

Spherocytosis, Type 5 Preferred

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