Trait
Delayed umbilical cord separation
Separation of the umbilical cord occurs at an abnormally late timepoint.
Summary
- Also called
- Delayed separation of umbilical cord
- Body system
- Abnormality of prenatal development or birth
This page as data
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page$trait$nameRead the genes linked to Delayed umbilical cord separation, and the rest of your genome, with one test.
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Get my Genome Test4 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Leukocyte Adhesion DeficiencyReads 1 of these genesITGB2About this report →
- Hyper-IgE SyndromeReads 1 of these genesIL6STAbout this report →
- Other Inborn Errors of ImmunityReads 3 of these genesMYD88RAC2IL6STAbout this report →
- Severe Combined ImmunodeficiencyReads 1 of these genesRAC2About this report →
Read the genes linked to Delayed umbilical cord separation, and the rest of your genome, with one test.
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Get my Genome Test5 genes linked to Delayed umbilical cord separation
Changes in these genes cause rare conditions in which Delayed umbilical cord separation is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ITGB2integrin subunit beta 2 | Always | In 1 condition |
| MYD88MYD88 innate immune signal transduction adaptor | Always | In 1 condition |
| RAC2Rac family small GTPase 2 | Always | In 1 condition |
| SMARCD2SWI/SNF related BAF chromatin remodeling complex subunit D2 | Always | In 1 condition |
| IL6STinterleukin 6 cytokine family signal transducer | Sometimes (5–29%) | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.19-9814e911.
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