Lesch-Nyhan Syndrome, Neurologic Variant MeSH Supplementary Concept Data 2025

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MeSH Supplementary: Lesch-Nyhan Syndrome, Neurologic Variant
Unique ID: C564535
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564535
Entry Term(s): HPRT Deficiency, Neurologic Variant
Registry Numbers: 0
Heading Mapped to: *Lesch-Nyhan Syndrome
Frequency: 1
Note: mutation in HPRT
Date of Entry: 2012/11/05
Revision Date: 2012/11/05

Lesch-Nyhan Syndrome, Neurologic Variant Preferred

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