Traits

Traits linked to PRMT7

protein arginine methyltransferase 7

The Human Phenotype Ontology links 87 traits to PRMT7, by body system: features seen in people with one of the gene's rare conditions.

Abnormality of head or neck

Trait	Cât de frecvent apare
Broad head shape	Întotdeauna
Decreased volume of lip	Întotdeauna
Flattened bony protrusion above eyes	Întotdeauna
Hairy forehead	Întotdeauna
Long philtrum	Întotdeauna
Redundant neck skin	Întotdeauna
Short neck	Întotdeauna
Abnormal facial shape	Foarte des (80–99%)
Flat face	Des (30–79%)
Flat nose	Des (30–79%)
Gum enlargement	Des (30–79%)
Nasal tip, upturned	Des (30–79%)
Prominent forehead	Des (30–79%)
Short nose	Des (30–79%)
Short opening between the eyelids	Des (30–79%)
Zygomatic flattening	Des (30–79%)
Abnormally small head	Uneori (5–29%)
Broad nasal tip	Uneori (5–29%)
Collapsed nostrils	Uneori (5–29%)
Dacryocystitis	Uneori (5–29%)
Dental crowding	Uneori (5–29%)
Depressed nasal bridge	Uneori (5–29%)
Eye folds	Uneori (5–29%)
Receding chin	Uneori (5–29%)
Skin tag in front of the ear	Uneori (5–29%)
Wide nasal bridge	Uneori (5–29%)
Frontal bossing	Neînregistrat
High palate	Neînregistrat

Abnormality of the nervous system

Trait	Cât de frecvent apare
Delayed ability to walk	Întotdeauna
Delayed CNS myelination	Întotdeauna
Delayed speech and language development	Întotdeauna
Global developmental delay	Întotdeauna
Severe global developmental delay	Întotdeauna
Short attention span	Întotdeauna
Sudden loss of muscle tone	Întotdeauna
Tethered cord	Întotdeauna
Intellectual disability	Foarte des (80–99%)
Abnormal shape of brain	Des (30–79%)
Epilepsy	Des (30–79%)
Intellectual disability, mild	Des (30–79%)
Intellectual disability, severe	Des (30–79%)
Specific learning disability	Des (30–79%)
Typical absence seizure	Des (30–79%)
Abnormal conus terminalis morphology	Uneori (5–29%)
IQ between 34 and 49	Uneori (5–29%)
Pauses in breathing while sleeping	Uneori (5–29%)
Seizure affecting one half of brain	Uneori (5–29%)
Thick corpus callosum	Uneori (5–29%)
Underdevelopment of part of brain called corpus callosum	Uneori (5–29%)

Abnormality of the eye

Trait	Cât de frecvent apare
Deeply set eye	Întotdeauna
Drooping upper eyelid	Întotdeauna
Astigmatism	Des (30–79%)
Cross-eyed	Des (30–79%)
Wide-set eyes	Des (30–79%)
Blue outer white part of eyeball	Uneori (5–29%)
Notched pupil	Uneori (5–29%)
Optic disc coloboma	Uneori (5–29%)

Abnormality of limbs

Trait	Cât de frecvent apare
Short long bone of foot	Întotdeauna
Short outermost finger bone	Întotdeauna
Short 4th long bone of foot	Foarte des (80–99%)
Short fingers or toes	Foarte des (80–99%)
Shortened long bone of hand	Des (30–79%)
Outward turned elbows	Uneori (5–29%)
Small kneecap	Uneori (5–29%)

Abnormality of the genitourinary system

Trait	Cât de frecvent apare
Frequent urinary tract infections	Întotdeauna
Small kidneys	Întotdeauna
Undescended testes	Des (30–79%)
Vesicoureteral reflux	Uneori (5–29%)

Growth abnormality

Trait	Cât de frecvent apare
Faltering weight	Întotdeauna
Prenatal growth deficiency	Întotdeauna
Short stature	Întotdeauna
Obesity	Des (30–79%)

Abnormality of the digestive system

Trait	Cât de frecvent apare
Acid reflux	Întotdeauna
Feeding difficulties	Întotdeauna
Rectum protrudes through anus	Întotdeauna

Abnormality of the integument

Trait	Cât de frecvent apare
Sparse hair	Întotdeauna
Spinal dimple	Întotdeauna
Soft skin	Uneori (5–29%)

Abnormality of the musculoskeletal system

Trait	Cât de frecvent apare
Abnormality of the skeletal system	Foarte des (80–99%)
Decreased muscle tone in infant	Foarte des (80–99%)
Low muscle tone	Foarte des (80–99%)

Abnormality of the endocrine system

Trait	Cât de frecvent apare
Pseudohypoparathyroidism	Des (30–79%)
Abnormality of the endocrine system	Uneori (5–29%)

Abnormality of prenatal development or birth

Trait	Cât de frecvent apare
High levels of amniotic fluid	Întotdeauna

Abnormality of the ear

Trait	Cât de frecvent apare
Sensorineural hearing impairment	Uneori (5–29%)

Abnormality of the immune system

Trait	Cât de frecvent apare
Eczema	Des (30–79%)

Abnormality of the respiratory system

Trait	Cât de frecvent apare
Softening of voice box tissue	Întotdeauna

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 PRMT7 and how often each is seen. Find out more at hpo.jax.org.

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