MeSH Browser

MeSH Supplementary: Uniparental disomy, paternal, chromosome 14
Unique ID: C536471
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536471
Entry Term(s): Kagami-Ogata syndrome; Paternal uniparental disomy 14
Registry Numbers: 0
Heading Mapped to: Chromosomes, Human, Pair 14; *Uniparental Disomy; *Imprinting Disorders
Frequency: 24
Date of Entry: 2010/08/25
Revision Date: 2023/05/31

Uniparental disomy, paternal, chromosome 14 MeSH Supplementary Concept Data 2025