Human Gene Set: HP_FETAL_NECK_ANOMALY


Standard name HP_FETAL_NECK_ANOMALY
Systematic name M45469
Brief description Fetal neck anomaly
Full description or abstract A structural anomaly in the fetal neck region. Terms in this subhierarchy are restricted to findings that can only be observed in the prenatal period. Other HPO terms can also be used to describe fetal phenotypes. []
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0025667
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0025667
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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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