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
Filtered by similarity ?
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  
Download gene set format: grp | gmt | xml | json | TSV metadata
Compute overlaps ? (show collections to investigate for overlap with this gene set)
Compendia expression profiles ? NG-CHM interactive heatmaps
(Please note that clustering takes a few seconds)
GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)

Legacy heatmaps (PNG)
GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
Advanced query Further investigate these 68 genes
Gene families ? Categorize these 68 genes by gene family
Show members (show 68 source identifiers mapped to 68 genes)
Version history 2025.1.Hs: Updated to HPO Release 2025-05-06.

See MSigDB license terms here. Please note that certain gene sets have special access terms.