Marked delay in bone age

3 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.

• Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesSTAT5BAbout this report →
• Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesLHX4About this report →
• Hypogonadotropic HypogonadismReads 1 of these genesLHX4About this report →

Every condition report

3 genes linked to Marked delay in bone age

Changes in these genes cause rare conditions in which Marked delay in bone age 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.

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 2026.10.17-8666dff2.