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Traits

Traits linked to FRYL

FRY like transcription coactivator

The Human Phenotype Ontology links 70 traits to FRYL, by body system: features seen in people with one of the gene's rare conditions.

Abnormality of the nervous system

TraitHvor ofte det ses
Abnormal social developmentAltid
AnxietyAltid
Attention deficitAltid
Borderline personality disorderAltid
Delayed speech and language developmentAltid
DepressionAltid
Difficulty sleepingAltid
Global developmental delayAltid
Intellectual disabilityAltid
Tic disorderAltid
AutismOfte (30–79 %)
Generalized-onset seizureOfte (30–79 %)
Seizure affecting one half of brainOfte (30–79 %)
Cortical dysplasiaNogle gange (5–29 %)
EpilepsyNogle gange (5–29 %)
Hippocampal malrotationNogle gange (5–29 %)
Thin corpus callosumNogle gange (5–29 %)

Abnormality of head or neck

TraitHvor ofte det ses
Downward slanting of the opening between the eyelidsAltid
Upward slanting of the opening between the eyelidsAltid
Abnormally small headNogle gange (5–29 %)
Almond shaped eyesNogle gange (5–29 %)
Depressed nasal bridgeNogle gange (5–29 %)
Eye foldsNogle gange (5–29 %)
Frontal bossingNogle gange (5–29 %)
Long faceNogle gange (5–29 %)
Long philtrumNogle gange (5–29 %)
Narrow foreheadNogle gange (5–29 %)
Nasal tip, upturnedNogle gange (5–29 %)
Pit in front of the earNogle gange (5–29 %)
Receding chinNogle gange (5–29 %)
Short noseNogle gange (5–29 %)
Short philtrumNogle gange (5–29 %)

Abnormality of the cardiovascular system

TraitHvor ofte det ses
Absent spleenAltid
Increased blood pressure in blood vessels of lungsAltid
Multiple small spleensAltid
Patent foramen ovaleOfte (30–79 %)
An opening in the wall separating the top two chambers of the heartNogle gange (5–29 %)
Heart tip and four chambers point towards right side of bodyNogle gange (5–29 %)
Hole in center of heartNogle gange (5–29 %)
Hole in heart wall separating two lower heart chambersNogle gange (5–29 %)
Interrupted aortic archNogle gange (5–29 %)
Narrowing of aortic valveNogle gange (5–29 %)
Narrowing of peripheral lung arteryNogle gange (5–29 %)
Narrowing of pulmonic valveNogle gange (5–29 %)
Patent ductus arteriosusNogle gange (5–29 %)
Tetralogy of FallotNogle gange (5–29 %)

Abnormality of the genitourinary system

TraitHvor ofte det ses
ChordeeAltid
Horseshoe kidneyAltid
Hydrocele testisAltid
HypospadiasAltid
Loss of bladder controlAltid
Undescended testesAltid

Abnormality of blood and blood-forming tissues

TraitHvor ofte det ses
Cancer of lymphatic systemAltid
Low platelet countAltid
Intraventricular hemorrhageNogle gange (5–29 %)

Abnormality of the digestive system

TraitHvor ofte det ses
Jejunal atresiaNogle gange (5–29 %)
MicrocolonNogle gange (5–29 %)
Midline liverNogle gange (5–29 %)

Abnormality of the ear

TraitHvor ofte det ses
Hearing impairmentAltid
Ears rotated toward back of headNogle gange (5–29 %)
Low-set earsNogle gange (5–29 %)

Growth abnormality

TraitHvor ofte det ses
Decreased body weightOfte (30–79 %)
Small for gestational ageOfte (30–79 %)
Short statureNogle gange (5–29 %)

Abnormality of the eye

TraitHvor ofte det ses
Deeply set eyeNogle gange (5–29 %)
Wide-set eyesNogle gange (5–29 %)

Abnormality of the integument

TraitHvor ofte det ses
Atypical nail growthNogle gange (5–29 %)
Spinal dimpleNogle gange (5–29 %)

Abnormality of the musculoskeletal system

TraitHvor ofte det ses
Pigeon chestAltid
Low muscle toneOfte (30–79 %)

Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.

Hvor oplysningerne kommer fra

  • The Human Phenotype Ontology, release 2026-09-01: the traits linked to FRYL and how often each is seen. Find out more at hpo.jax.org.

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