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Traits
Traits linked to CDSN
corneodesmosin
The Human Phenotype Ontology links 29 traits to CDSN, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Itching | Always |
| Scaling skin | Always |
| Fine hair | Very often (80–99%) |
| Brittle hair | Often (30–79%) |
| Hyperkeratosis | Often (30–79%) |
| Parakeratosis | Often (30–79%) |
| Thickening of upper layer of skin | Often (30–79%) |
| Detachment of nail | Sometimes (5–29%) |
| Poor nail formation | Sometimes (5–29%) |
| Abnormality of the axillary hair | Not recorded |
| Abnormality of the nail | Not recorded |
| Abnormality of the pubic hair | Not recorded |
| Absent facial hair | Not recorded |
| Cleavage at junction of stratum corneum and stratum granulosum | Not recorded |
| Generalized hypotrichosis | Not recorded |
| Lack of sweating or excessive sweating | Not recorded |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Sparse scalp hair | Always |
| Slow-growing scalp hair | Very often (80–99%) |
| Absence of scalp hair | Often (30–79%) |
| Hay fever | Sometimes (5–29%) |
| Abnormal dentition | Not recorded |
| Abnormal eyelashes | Not recorded |
| Abnormality of the eyebrow | Not recorded |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Red scaly skin caused by inflammatory skin disease | Always |
| Asthma | Sometimes (5–29%) |
| Baby eczema | Sometimes (5–29%) |
Abnormal cellular phenotype
| Trait | How often it is seen |
|---|---|
| Increased circulating IgE concentration | Always |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| High blood eosinophil count | Always |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Excessive sweating of palms and soles | 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 CDSN and how often each is seen. Find out more at hpo.jax.org.
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