Traits

Traits linked to ZBTB42

zinc finger and BTB domain containing 42

The Human Phenotype Ontology links 6 traits to ZBTB42, by body system: features seen in people with one of the gene's rare conditions.

Abnormality of prenatal development or birth

Trait	How often it is seen
Absence of stomach bubble on fetal sonography	Always
High levels of amniotic fluid	Always
Less than 10 fetal movements in 12 hours	Always

Abnormality of the musculoskeletal system

Trait	How often it is seen
Arthrogryposis multiplex congenita	Always
Congenital contracture	Always

Abnormality of head or neck

Trait	How often it is seen
Big calvaria	Often (30–79%)

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.

Where this comes from

The Human Phenotype Ontology, release 2026-09-01: the traits linked to ZBTB42 and how often each is seen. Find out more at hpo.jax.org.

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