Human Gene Set: HP_ABNORMAL_FETAL_SKIN_MORPHOLOGY


Standard name HP_ABNORMAL_FETAL_SKIN_MORPHOLOGY
Systematic name M45470
Brief description Abnormal fetal skin morphology
Full description or abstract Any structural anomaly of the skin of the fetus or newborn. 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:0025723
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0025723
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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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