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Traits
Traits linked to NOG
noggin
The Human Phenotype Ontology links 102 traits to NOG, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of limbs
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Thin red part of the upper lip | Very often (80–99%) |
| Limited neck range of motion | Often (30–79%) |
| Long nose | Often (30–79%) |
| Low hanging columella | Often (30–79%) |
| Underdeveloped tissue around nostril | Often (30–79%) |
| Wide nasal bridge | Often (30–79%) |
| Asymmetry of the mouth | Sometimes (5–29%) |
| Facial asymmetry | Sometimes (5–29%) |
| Upward slanting of the opening between the eyelids | Sometimes (5–29%) |
| Decreased size of nasal septum | Not recorded |
| Full upper lip | Not recorded |
| Narrow face | Not recorded |
| Short philtrum | Not recorded |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Joint stiffness | Very often (80–99%) |
| Proximal symphalangism | Very often (80–99%) |
| Cone-shaped end part of bone | Often (30–79%) |
| Fused neck | Often (30–79%) |
| Enlargement of the costochondral junction | Not recorded |
| Funnel chest | Not recorded |
| Narrow spinal canal | Not recorded |
| Short sternum | Not recorded |
| Underdeveloped spinal processes | Not recorded |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Conductive deafness | Very often (80–99%) |
| Congenital stapes ankylosis | Very often (80–99%) |
| Stapes ankylosis | Very often (80–99%) |
| Sensorineural hearing impairment | Often (30–79%) |
| Bilateral conductive hearing impairment | Sometimes (5–29%) |
| Hearing abnormality | Sometimes (5–29%) |
| Progressive conductive hearing impairment | Not recorded |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Farsightedness | Very often (80–99%) |
| Drooping upper eyelid | Often (30–79%) |
| Astigmatism | Sometimes (5–29%) |
| Cross-eyed | Sometimes (5–29%) |
| Lazy eye | Sometimes (5–29%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Absent fingernail | Very often (80–99%) |
| Absent/small nails | Often (30–79%) |
| Abnormality of the nail | Sometimes (5–29%) |
| Absent nails | Not recorded |
| Absent/small toenails | Not recorded |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Waddling gait | Sometimes (5–29%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Short stature | Very often (80–99%) |
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 NOG and how often each is seen. Find out more at hpo.jax.org.
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