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	Cât de frecvent apare
Abnormal social development	Întotdeauna
Anxiety	Întotdeauna
Attention deficit	Întotdeauna
Borderline personality disorder	Întotdeauna
Delayed speech and language development	Întotdeauna
Depression	Întotdeauna
Difficulty sleeping	Întotdeauna
Global developmental delay	Întotdeauna
Intellectual disability	Întotdeauna
Tic disorder	Întotdeauna
Autism	Des (30–79%)
Generalized-onset seizure	Des (30–79%)
Seizure affecting one half of brain	Des (30–79%)
Cortical dysplasia	Uneori (5–29%)
Epilepsy	Uneori (5–29%)
Hippocampal malrotation	Uneori (5–29%)
Thin corpus callosum	Uneori (5–29%)

Abnormality of head or neck

Trait	Cât de frecvent apare
Downward slanting of the opening between the eyelids	Întotdeauna
Upward slanting of the opening between the eyelids	Întotdeauna
Abnormally small head	Uneori (5–29%)
Almond shaped eyes	Uneori (5–29%)
Depressed nasal bridge	Uneori (5–29%)
Eye folds	Uneori (5–29%)
Frontal bossing	Uneori (5–29%)
Long face	Uneori (5–29%)
Long philtrum	Uneori (5–29%)
Narrow forehead	Uneori (5–29%)
Nasal tip, upturned	Uneori (5–29%)
Pit in front of the ear	Uneori (5–29%)
Receding chin	Uneori (5–29%)
Short nose	Uneori (5–29%)
Short philtrum	Uneori (5–29%)

Abnormality of the cardiovascular system

Trait	Cât de frecvent apare
Absent spleen	Întotdeauna
Increased blood pressure in blood vessels of lungs	Întotdeauna
Multiple small spleens	Întotdeauna
Patent foramen ovale	Des (30–79%)
An opening in the wall separating the top two chambers of the heart	Uneori (5–29%)
Heart tip and four chambers point towards right side of body	Uneori (5–29%)
Hole in center of heart	Uneori (5–29%)
Hole in heart wall separating two lower heart chambers	Uneori (5–29%)
Interrupted aortic arch	Uneori (5–29%)
Narrowing of aortic valve	Uneori (5–29%)
Narrowing of peripheral lung artery	Uneori (5–29%)
Narrowing of pulmonic valve	Uneori (5–29%)
Patent ductus arteriosus	Uneori (5–29%)
Tetralogy of Fallot	Uneori (5–29%)

Abnormality of the genitourinary system

Trait	Cât de frecvent apare
Chordee	Întotdeauna
Horseshoe kidney	Întotdeauna
Hydrocele testis	Întotdeauna
Hypospadias	Întotdeauna
Loss of bladder control	Întotdeauna
Undescended testes	Întotdeauna

Abnormality of blood and blood-forming tissues

Trait	Cât de frecvent apare
Cancer of lymphatic system	Întotdeauna
Low platelet count	Întotdeauna
Intraventricular hemorrhage	Uneori (5–29%)

Abnormality of the digestive system

Trait	Cât de frecvent apare
Jejunal atresia	Uneori (5–29%)
Microcolon	Uneori (5–29%)
Midline liver	Uneori (5–29%)

Abnormality of the ear

Trait	Cât de frecvent apare
Hearing impairment	Întotdeauna
Ears rotated toward back of head	Uneori (5–29%)
Low-set ears	Uneori (5–29%)

Growth abnormality

Trait	Cât de frecvent apare
Decreased body weight	Des (30–79%)
Small for gestational age	Des (30–79%)
Short stature	Uneori (5–29%)

Abnormality of the eye

Trait	Cât de frecvent apare
Deeply set eye	Uneori (5–29%)
Wide-set eyes	Uneori (5–29%)

Abnormality of the integument

Trait	Cât de frecvent apare
Atypical nail growth	Uneori (5–29%)
Spinal dimple	Uneori (5–29%)

Abnormality of the musculoskeletal system

Trait	Cât de frecvent apare
Pigeon chest	Întotdeauna
Low muscle tone	Des (30–79%)

Cât de frecvent apare în rândul persoanelor cu una dintre afecțiunile asociate genei, cel mai des întâlnit dintre acestea, conform Human Phenotype Ontology. Aceste pagini descriu trăsături și cercetările din spatele lor; ele nu reprezintă un diagnostic, iar pentru simptome trebuie să vă adresați medicului sau consilierului genetic.

De unde provin aceste informații

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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