Kallmann Syndrome 6 MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Kallmann Syndrome 6
Unique ID: C567199
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567199
Heading Mapped to: *Kallmann Syndrome
Frequency: 0
Note: mutation in FGF8
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Kallmann Syndrome 6 Preferred

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