Human Gene Set: HP_ABNORMALITY_OF_THE_UMBILICAL_CORD


Standard name HP_ABNORMALITY_OF_THE_UMBILICAL_CORD
Systematic name M37682
Brief description Abnormality of the umbilical cord
Full description or abstract An abnormality of the umbilical cord, which is the cord connecting the developing embryo or fetus to the placenta. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0010881
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0010881
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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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NCI-60 cell lines (National Cancer Institute)
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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