Traits

Traits linked to FOXJ1

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The Human Phenotype Ontology links 50 traits to FOXJ1, by body system: features seen in people with one of the gene's rare conditions.

Abnormality of the cardiovascular system

Trait	Kaip dažnai pasireiškia
Abnormal cardiovascular system morphology	Kartais (5–29%)
Abnormality of the heart	Kartais (5–29%)
All organs on wrong side of body	Kartais (5–29%)
Abnormal inferior vena cava morphology	Retai (1–4 %)
Abnormal location of heart atrium	Retai (1–4 %)
Absent spleen	Retai (1–4 %)
Anomalous pulmonary venous return	Retai (1–4 %)
Atrial situs ambiguous	Retai (1–4 %)
Double outlet right ventricle	Retai (1–4 %)
Multiple small spleens	Retai (1–4 %)
Persistent left superior vena cava	Retai (1–4 %)
Transposition of the great arteries	Retai (1–4 %)

Abnormality of the respiratory system

Trait	Kaip dažnai pasireiškia
Permanent enlargement of the airways of the lungs	Visada
Wet cough	Visada
Abnormal sputum	Dažnai (30–79%)
Neonatal respiratory distress	Dažnai (30–79%)
Respiratory tract infection	Dažnai (30–79%)
Lithoptysis	Kartais (5–29%)
Obstructive lung disease	Kartais (5–29%)
Partial or complete collapse of part or entire lung	Kartais (5–29%)
Peribronchovascular interstitial thickening	Kartais (5–29%)
Pulmonary situs ambiguus	Kartais (5–29%)
Wheezing	Kartais (5–29%)
Respiratory failure	Retai (1–4 %)

Abnormality of head or neck

Trait	Kaip dažnai pasireiškia
Chronic rhinitis	Visada
Chronic sinus disease	Visada
Recurrent colds	Visada
Blockage of nose	Dažnai (30–79%)
Nasal polyposis	Dažnai (30–79%)

Abnormality of the nervous system

Trait	Kaip dažnai pasireiškia
Noncommunicating hydrocephalus	Visada
Delayed speech and language development	Kartais (5–29%)
Morphological central nervous system abnormality	Kartais (5–29%)
Too much cerebrospinal fluid in the brain	Retai (1–4 %)
Ventriculomegaly	Retai (1–4 %)

Abnormality of the ear

Trait	Kaip dažnai pasireiškia
Chronic infections of the middle ear	Dažnai (30–79%)
Recurrent middle ear infection	Dažnai (30–79%)
Conductive deafness	Kartais (5–29%)
Hearing impairment	Kartais (5–29%)

Abnormality of the genitourinary system

Trait	Kaip dažnai pasireiškia
Abnormal sperm motility	Dažnai (30–79%)
Male infertility	Dažnai (30–79%)
Abnormality of the genitourinary system	Kartais (5–29%)
Female infertility	Kartais (5–29%)

Abnormality of the immune system

Trait	Kaip dažnai pasireiškia
Recurrent chest infections	Visada
Recurrent sinus and lung infections	Dažnai (30–79%)
Recurrent mycobacterial infections	Kartais (5–29%)

Abnormality of the digestive system

Trait	Kaip dažnai pasireiškia
Abdominal situs inversus	Dažnai (30–79%)
Intestinal malrotation	Retai (1–4 %)

Abnormality of limbs

Trait	Kaip dažnai pasireiškia
Clubbing of fingers and toes	Kartais (5–29%)

Abnormality of the eye

Trait	Kaip dažnai pasireiškia
Rod-cone dystrophy	Retai (1–4 %)

Abnormality of the musculoskeletal system

Trait	Kaip dažnai pasireiškia
Abnormality of the skeletal system	Kartais (5–29%)

Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.

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The Human Phenotype Ontology, release 2026-09-01: the traits linked to FOXJ1 and how often each is seen. Find out more at hpo.jax.org.

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