Human Gene Set: HP_ISOMERISM


Standard name HP_ISOMERISM
Systematic name M43518
Brief description Isomerism
Full description or abstract Isomerism in the context of the congenitally malformed heart is defined as a situation where some paired structures on opposite sides of the left-right axis of the body are, in morphologic terms, symmetrical mirror images of each other. [PMID:21731561]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0031853
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0031853
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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