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

Trait	Hvor ofte den forekommer
Abnormal social development	Alltid
Anxiety	Alltid
Attention deficit	Alltid
Borderline personality disorder	Alltid
Delayed speech and language development	Alltid
Depression	Alltid
Difficulty sleeping	Alltid
Global developmental delay	Alltid
Intellectual disability	Alltid
Tic disorder	Alltid
Autism	Ofte (30–79 %)
Generalized-onset seizure	Ofte (30–79 %)
Seizure affecting one half of brain	Ofte (30–79 %)
Cortical dysplasia	Noen ganger (5–29 %)
Epilepsy	Noen ganger (5–29 %)
Hippocampal malrotation	Noen ganger (5–29 %)
Thin corpus callosum	Noen ganger (5–29 %)

Abnormality of head or neck

Trait	Hvor ofte den forekommer
Downward slanting of the opening between the eyelids	Alltid
Upward slanting of the opening between the eyelids	Alltid
Abnormally small head	Noen ganger (5–29 %)
Almond shaped eyes	Noen ganger (5–29 %)
Depressed nasal bridge	Noen ganger (5–29 %)
Eye folds	Noen ganger (5–29 %)
Frontal bossing	Noen ganger (5–29 %)
Long face	Noen ganger (5–29 %)
Long philtrum	Noen ganger (5–29 %)
Narrow forehead	Noen ganger (5–29 %)
Nasal tip, upturned	Noen ganger (5–29 %)
Pit in front of the ear	Noen ganger (5–29 %)
Receding chin	Noen ganger (5–29 %)
Short nose	Noen ganger (5–29 %)
Short philtrum	Noen ganger (5–29 %)

Abnormality of the cardiovascular system

Trait	Hvor ofte den forekommer
Absent spleen	Alltid
Increased blood pressure in blood vessels of lungs	Alltid
Multiple small spleens	Alltid
Patent foramen ovale	Ofte (30–79 %)
An opening in the wall separating the top two chambers of the heart	Noen ganger (5–29 %)
Heart tip and four chambers point towards right side of body	Noen ganger (5–29 %)
Hole in center of heart	Noen ganger (5–29 %)
Hole in heart wall separating two lower heart chambers	Noen ganger (5–29 %)
Interrupted aortic arch	Noen ganger (5–29 %)
Narrowing of aortic valve	Noen ganger (5–29 %)
Narrowing of peripheral lung artery	Noen ganger (5–29 %)
Narrowing of pulmonic valve	Noen ganger (5–29 %)
Patent ductus arteriosus	Noen ganger (5–29 %)
Tetralogy of Fallot	Noen ganger (5–29 %)

Abnormality of the genitourinary system

Trait	Hvor ofte den forekommer
Chordee	Alltid
Horseshoe kidney	Alltid
Hydrocele testis	Alltid
Hypospadias	Alltid
Loss of bladder control	Alltid
Undescended testes	Alltid

Abnormality of blood and blood-forming tissues

Trait	Hvor ofte den forekommer
Cancer of lymphatic system	Alltid
Low platelet count	Alltid
Intraventricular hemorrhage	Noen ganger (5–29 %)

Abnormality of the digestive system

Trait	Hvor ofte den forekommer
Jejunal atresia	Noen ganger (5–29 %)
Microcolon	Noen ganger (5–29 %)
Midline liver	Noen ganger (5–29 %)

Abnormality of the ear

Trait	Hvor ofte den forekommer
Hearing impairment	Alltid
Ears rotated toward back of head	Noen ganger (5–29 %)
Low-set ears	Noen ganger (5–29 %)

Growth abnormality

Trait	Hvor ofte den forekommer
Decreased body weight	Ofte (30–79 %)
Small for gestational age	Ofte (30–79 %)
Short stature	Noen ganger (5–29 %)

Abnormality of the eye

Trait	Hvor ofte den forekommer
Deeply set eye	Noen ganger (5–29 %)
Wide-set eyes	Noen ganger (5–29 %)

Abnormality of the integument

Trait	Hvor ofte den forekommer
Atypical nail growth	Noen ganger (5–29 %)
Spinal dimple	Noen ganger (5–29 %)

Abnormality of the musculoskeletal system

Trait	Hvor ofte den forekommer
Pigeon chest	Alltid
Low muscle tone	Ofte (30–79 %)

Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.

Slik er informasjonen samlet

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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