Traits

Traits linked to SLC10A7

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The Human Phenotype Ontology links 37 traits to SLC10A7, by body system: features seen in people with one of the gene's rare conditions.

Abnormality of the musculoskeletal system

Trait	How often it is seen
Double-Jointed	Often (30–79%)
Scoliosis	Often (30–79%)
Coronal cleft vertebrae	Sometimes (5–29%)
Irregular vertebral endplates	Sometimes (5–29%)
Advanced bone age	Not recorded
Flat end part of bone	Not recorded
Kyphoscoliosis	Not recorded
Prominent swayback	Not recorded
Short long bone	Not recorded
Shorter than typical length between neck and abdomen	Not recorded
Small chest	Not recorded
Small end part of bone	Not recorded

Abnormality of head or neck

Trait	How often it is seen
Amelogenesis imperfecta	Always
Thin dental enamel	Always
Little lower jaw	Very often (80–99%)
Dental cavities	Often (30–79%)
Big lower jaw	Sometimes (5–29%)
Cleft palate	Sometimes (5–29%)
Decreased number of teeth	Rarely (1–4%)
Pierre-Robin sequence	Rarely (1–4%)
High palate	Not recorded
Round face	Not recorded
Small retruded chin	Not recorded

Abnormality of limbs

Trait	How often it is seen
Coxa valga	Often (30–79%)
Knock knees	Often (30–79%)
Dropped arches	Rarely (1–4%)
Accelerated wrist bone maturation	Not recorded
Hip contracture	Not recorded
Knee dislocation	Not recorded
Short neck of thighbone	Not recorded

Growth abnormality

Trait	How often it is seen
Short stature	Always
Obesity	Rarely (1–4%)
Truncal obesity	Rarely (1–4%)
Disproportionate short stature	Not recorded

Abnormality of the digestive system

Trait	How often it is seen
Inguinal hernia	Often (30–79%)

Abnormality of the ear

Trait	How often it is seen
Hearing impairment	Always

Abnormality of the nervous system

Trait	How often it is seen
Global developmental delay	Rarely (1–4%)

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 SLC10A7 and how often each is seen. Find out more at hpo.jax.org.

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