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Traits

Traits linked to WNT10A

Wnt family member 10A

The Human Phenotype Ontology links 82 traits to WNT10A, by body system: features seen in people with one of the gene's rare conditions.

Abnormality of head or neck

TraitHvor ofte det ses
Absence of adult teethAltid
Failure of development of between one and six teethAltid
Failure of development of more than six teethAltid
Multiple eyelid margin cystsAltid
Wide gaps between baby teethAltid
Chewing difficultiesMeget ofte (80–99 %)
Decreased size of teethMeget ofte (80–99 %)
Early loss of baby teethMeget ofte (80–99 %)
Abnormality of baby teethOfte (30–79 %)
Abnormality of dental shapeOfte (30–79 %)
Absence of premolarOfte (30–79 %)
Absence of six year molarOfte (30–79 %)
Absence of upper lateral incisorOfte (30–79 %)
Absent central incisorOfte (30–79 %)
Bad biteOfte (30–79 %)
Cone shaped front toothOfte (30–79 %)
Decreased length of dental rootsOfte (30–79 %)
Decreased size of toothOfte (30–79 %)
Delayed eruption of permanent teethOfte (30–79 %)
Delayed eruption of teethOfte (30–79 %)
Short eyelashesOfte (30–79 %)
Smooth tongueOfte (30–79 %)
Sparse eyebrowOfte (30–79 %)
Sparse or absent eyebrowsOfte (30–79 %)
Sparse scalp hairOfte (30–79 %)
Widely spaced teethOfte (30–79 %)
Abnormality of canineNogle gange (5–29 %)
Abnormality of shape of baby molarNogle gange (5–29 %)
Absence of lower premolarNogle gange (5–29 %)
Bird-like facial appearanceNogle gange (5–29 %)
Cleft of the mouthNogle gange (5–29 %)
Outward turned lipsNogle gange (5–29 %)
Peg-shaped maxillary lateral incisorsNogle gange (5–29 %)
Short faceNogle gange (5–29 %)
TaurodontiaNogle gange (5–29 %)
Thin dental enamelNogle gange (5–29 %)
Decreased number of teethIkke registreret

Abnormality of the integument

TraitHvor ofte det ses
Dry skinAltid
HyperkeratosisAltid
Poor fingernail formationAltid
Poor nail formationAltid
Short nailAltid
Sparse body hairAltid
Sparse hairAltid
Abnormal fingernailsMeget ofte (80–99 %)
Abnormality of the hairMeget ofte (80–99 %)
Abnormality of the toenailMeget ofte (80–99 %)
Ectodermal dysplasiaMeget ofte (80–99 %)
Fine hairMeget ofte (80–99 %)
Decreased ability to sweatOfte (30–79 %)
Follicular hyperkeratosisOfte (30–79 %)
Grooved nailsOfte (30–79 %)
Hair lossOfte (30–79 %)
Poor toenail formationOfte (30–79 %)
Thin nailOfte (30–79 %)
Basal cell carcinomaNogle gange (5–29 %)
Excessive sweatingNogle gange (5–29 %)
Squamous cell carcinomaNogle gange (5–29 %)
Thin skinNogle gange (5–29 %)
Absent nailsIkke registreret
Apocrine hidrocystomaIkke registreret
Atypical nail growthIkke registreret
Chicken skinIkke registreret
Detachment of nailIkke registreret
Dry hairIkke registreret
HypergranulosisIkke registreret
Narrow nailIkke registreret
OrthokeratosisIkke registreret
PoromaIkke registreret
Small nailIkke registreret
Thickening of upper layer of skinIkke registreret

Abnormality of limbs

TraitHvor ofte det ses
Thickening of palms and solesAltid
Excessive sweating of palms and solesOfte (30–79 %)
Plantar hyperkeratosisOfte (30–79 %)
Thickening of the outer layer of the skin of the palms and solesOfte (30–79 %)
Palmar hyperkeratosisNogle gange (5–29 %)

Abnormality of the cardiovascular system

TraitHvor ofte det ses
Facial telangiectasiaMeget ofte (80–99 %)
Palmoplantar erythemaOfte (30–79 %)
Redness of skin or mucous membraneIkke registreret

Abnormality of the eye

TraitHvor ofte det ses
Extreme sensitivity of the eyes to lightOfte (30–79 %)
Abnormality of the eyeIkke registreret

Abnormality of the genitourinary system

TraitHvor ofte det ses
Ovarian cancerNogle gange (5–29 %)

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 WNT10A and how often each is seen. Find out more at hpo.jax.org.

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