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Traits
Traits linked to IL17RD
interleukin 17 receptor D
The Human Phenotype Ontology links 50 traits to IL17RD, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Abnormal erection | Very often (80–99%) |
| Decreased fertility | Very often (80–99%) |
| Decreased testicular size | Very often (80–99%) |
| Short penis | Very often (80–99%) |
| Underdeveloped penis | Very often (80–99%) |
| Undescended testes | Often (30–79%) |
| Abnormal morphology of female internal genitalia | Sometimes (5–29%) |
| Absent kidney | Sometimes (5–29%) |
| Dyspareunia | Sometimes (5–29%) |
| Primary amenorrhea | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Low solidness and mass of the bones | Often (30–79%) |
| Abnormal skeletal development | Sometimes (5–29%) |
| Delayed bone maturation | Sometimes (5–29%) |
| Low muscle tone | Sometimes (5–29%) |
| Muscle weakness | Sometimes (5–29%) |
| Osteopenia | Sometimes (5–29%) |
| Osteoporosis | Sometimes (5–29%) |
| Recurrent fractures | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Abnormal gait | Sometimes (5–29%) |
| Ataxia | Sometimes (5–29%) |
| Difficulty articulating speech | Sometimes (5–29%) |
| Epilepsy | Sometimes (5–29%) |
| Hand mirror movements | Sometimes (5–29%) |
| Leg paralysis | Sometimes (5–29%) |
| Tremor | Sometimes (5–29%) |
Abnormality of the endocrine system
| Trait | How often it is seen |
|---|---|
| Absence of pubertal development | Very often (80–99%) |
| Anterior hypopituitarism | Very often (80–99%) |
| Delayed puberty | Very often (80–99%) |
| Gonadotropin-releasing hormone deficiency | Very often (80–99%) |
| Hypogonadotropic hypogonadism | Very often (80–99%) |
| Decreased activity of gonads | Not recorded |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Lost smell | Always |
| Hyposmia | Very often (80–99%) |
| Abnormal dentition | Sometimes (5–29%) |
| Cleft palate | Sometimes (5–29%) |
| Decreased number of teeth | Sometimes (5–29%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Abnormal color vision | Sometimes (5–29%) |
| Drooping upper eyelid | Sometimes (5–29%) |
| Involuntary, rapid, rhythmic eye movements | Sometimes (5–29%) |
| Visual impairment | Sometimes (5–29%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Dropped arches | Sometimes (5–29%) |
| High-arched foot | Sometimes (5–29%) |
Abnormality of the breast
| Trait | How often it is seen |
|---|---|
| Underdeveloped breasts | Often (30–79%) |
| Enlarged male breast | Sometimes (5–29%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Hearing impairment | Often (30–79%) |
| Sensorineural hearing impairment | Sometimes (5–29%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Abnormal cardiovascular system morphology | Sometimes (5–29%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Ichthyosis | Sometimes (5–29%) |
Abnormality of the voice
| Trait | How often it is seen |
|---|---|
| Abnormality of the voice | Often (30–79%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Obesity | 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 IL17RD and how often each is seen. Find out more at hpo.jax.org.
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