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Traits

Traits linked to TTI2

TELO2 interacting protein 2

The Human Phenotype Ontology links 33 traits to TTI2, by body system: features seen in people with one of the gene's rare conditions.

Abnormality of the nervous system

TraitHvor ofte det ses
Aggressive behaviorAltid
Delayed ability to walkAltid
Delayed speech and language developmentAltid
Intellectual disability, severeAltid
IQ between 34 and 49Altid
More active than typicalAltid
Repetitive movementsAltid
Global developmental delayMeget ofte (80–99 %)
Behavioral abnormalityOfte (30–79 %)
Difficulty sleepingOfte (30–79 %)
Abnormal cerebral white matter morphologyNogle gange (5–29 %)
IrritabilityNogle gange (5–29 %)
Underdevelopment of part of brain called corpus callosumNogle gange (5–29 %)

Abnormality of head or neck

TraitHvor ofte det ses
Abnormally small headAltid
Abnormal facial shapeMeget ofte (80–99 %)
Bad biteOfte (30–79 %)
Abnormal dentitionNogle gange (5–29 %)
Decreased volume of lipNogle gange (5–29 %)
MonobrowNogle gange (5–29 %)
Prominent noseNogle gange (5–29 %)
Sloping foreheadNogle gange (5–29 %)

Abnormality of the musculoskeletal system

TraitHvor ofte det ses
KyphoscoliosisAltid
ScoliosisOfte (30–79 %)
MyotoniaNogle gange (5–29 %)

Abnormality of limbs

TraitHvor ofte det ses
BunionOfte (30–79 %)
Webbed 2nd and 3rd toesNogle gange (5–29 %)

Abnormality of the ear

TraitHvor ofte det ses
Large earsNogle gange (5–29 %)
Anteverted earsIkke registreret

Abnormality of the eye

TraitHvor ofte det ses
Cross-eyedNogle gange (5–29 %)
Deeply set eyeNogle gange (5–29 %)

Abnormality of blood and blood-forming tissues

TraitHvor ofte det ses
Decreased blood lymphocyte numberNogle gange (5–29 %)

Abnormality of the genitourinary system

TraitHvor ofte det ses
Early menopauseNogle gange (5–29 %)

Growth abnormality

TraitHvor ofte det ses
Short statureAltid

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 TTI2 and how often each is seen. Find out more at hpo.jax.org.

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