Traits

Traits linked to NEMF

nuclear export mediator factor

The Human Phenotype Ontology links 10 traits to NEMF, by body system: features seen in people with one of the gene's rare conditions.

Abnormality of the nervous system

Trait	How often it is seen
Delayed speech and language development	Always
Peripheral axonal neuropathy	Always
Ataxia	Often (30–79%)
Global developmental delay	Often (30–79%)
Intellectual disability	Often (30–79%)
Tremor	Sometimes (5–29%)

Abnormality of the musculoskeletal system

Trait	How often it is seen
Distal muscle wasting	Often (30–79%)
Generalized decreased muscle tone	Often (30–79%)
Kyphoscoliosis	Often (30–79%)

Abnormality of the respiratory system

Trait	How often it is seen
Breathing difficulties	Sometimes (5–29%)

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 NEMF and how often each is seen. Find out more at hpo.jax.org.

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