Human Gene Set: HP_FETAL_ANOMALY


Standard name HP_FETAL_ANOMALY
Systematic name M45502
Brief description Fetal anomaly
Full description or abstract Structural or functional abnormalities of the fetus. Note that this section comprises terms that describe abnormalities that are specific to the fetus or differ from the corresponding general terms. A term from anywhere in the Human Phenotype Ontology can be applied to a fetus if appropriate. []
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0034057
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0034057
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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
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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