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Traits
Traits linked to SCARF2
scavenger receptor class F member 2
The Human Phenotype Ontology links 76 traits to SCARF2, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Bunion | Always |
| Camptodactyly of 2nd-5th fingers | Always |
| Distal ulnar hypoplasia | Always |
| Dropped arches | Always |
| Elbow flexion contracture | Always |
| Knock knees | Always |
| Long big toe | Always |
| Radioulnar subluxation | Always |
| Recurrent patellar dislocation | Always |
| Tapered finger | Always |
| Webbed skin of 2nd-3rd toes | Always |
| Long slender fingers | Very often (80–99%) |
| Bowing of the long bones | Often (30–79%) |
| Dislocated radial head | Often (30–79%) |
| Long foot | Often (30–79%) |
| Slender long bones of hand | Often (30–79%) |
| Webbed 2nd and 3rd toes | Often (30–79%) |
| Club feet | Sometimes (5–29%) |
| Curvature of digit | Sometimes (5–29%) |
| Knee contracture | Sometimes (5–29%) |
| Bowed thighbone | Not recorded |
| Camptodactyly of toe | Not recorded |
| Curving of inner forearm bone | Not recorded |
| Elongated long bone of hand | Not recorded |
| Inability to straighten knee | Not recorded |
| Joint contracture of the hand | Not recorded |
| Narrow foot | Not recorded |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Beaked nose | Always |
| Decreased size of maxilla | Always |
| Depressed nasal bridge | Always |
| Drooping lower lip | Always |
| High palate | Always |
| High, narrow palate | Always |
| Little lower jaw | Always |
| Narrow mouth | Always |
| Narrow nose | Always |
| Narrow opening between the eyelids | Always |
| Scaphocephaly | Always |
| Triangular face | Always |
| Zygomatic flattening | Very often (80–99%) |
| Downward slanting of the opening between the eyelids | Often (30–79%) |
| Facial asymmetry | Often (30–79%) |
| Abnormal columella morphology | Sometimes (5–29%) |
| Deformity of the skull | Sometimes (5–29%) |
| Dental crowding | Sometimes (5–29%) |
| Deviated nasal septum | Sometimes (5–29%) |
| Underdeveloped tissue around nostril | Sometimes (5–29%) |
| Abnormality of the eyebrow | Not recorded |
| Cleft palate | Not recorded |
| Narrowing of the rear opening of the nasal cavity | Not recorded |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Double-Jointed | Always |
| Elbow contracture | Always |
| Hook-shaped collarbone | Always |
| Permanent flexion of the finger or toe | Always |
| Joint contracture | Often (30–79%) |
| Thin ribs | Often (30–79%) |
| Glenoid fossa hypoplasia | Sometimes (5–29%) |
| Short collarbone | Sometimes (5–29%) |
| Short ribs | Sometimes (5–29%) |
| Small shoulder blade | Sometimes (5–29%) |
| Funnel chest | Not recorded |
| Slender long bone | Not recorded |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Small earlobe | Always |
| Ears rotated toward back of head | Often (30–79%) |
| Overfolded ears | Often (30–79%) |
| Prominent ear | Often (30–79%) |
| Hearing impairment | Sometimes (5–29%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Abnormal aryepiglottic fold morphology | Sometimes (5–29%) |
| Noisy breathing | Not recorded |
| Softening of voice box tissue | Not recorded |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Dilatation of the renal pelvis | Sometimes (5–29%) |
| Hydronephrosis | Sometimes (5–29%) |
Abnormality of prenatal development or birth
| Trait | How often it is seen |
|---|---|
| Only one artery in umbilical cord instead of two | Not recorded |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Hardening of skin and connective tissue | Sometimes (5–29%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Spinal dimple | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Delayed speech and language development | 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 SCARF2 and how often each is seen. Find out more at hpo.jax.org.
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