204100.6.2

Country

Tunisia

HPO Terms

Retinal dystrophy; Progressive visual loss; Congenital stationary night blindness; Congenital nystagmus; Severely reduced visual acuity
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Sex

Female

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_000329.2:c.271C>T2

Remarks

Brother of 204100.6.1

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
204100.6.1TunisiaRetinal dystrophy; Progressive visual loss; Congenital stationary night blindness; Congenital nystagmus; Severely reduced visual acuityFemaleYesYes
204100.6.3TunisiaRetinal dystrophy; Progressive visual loss; Congenital stationary night blindness; Congenital nystagmus; Severely reduced visual acuityFemaleYesYesSecond cousin of 204100.6.1
204100.6.4TunisiaRetinal dystrophy; Progressive visual loss; Congenital stationary night blindness; Congenital nystagmus; Severely reduced visual acuityMaleYesYesSecond cousin of 204100.6.1; Brother of 204100.6.3
204100.6.5TunisiaRetinal dystrophy; Progressive visual loss; Congenital stationary night blindness; Congenital nystagmus; Severely reduced visual acuityMaleYesYesSecond cousin of 204100.6.1; Brother of 204100.6.3
204100.6.6TunisiaRetinal dystrophy; Progressive visual loss; Congenital stationary night blindness; Congenital nystagmus; Severely reduced visual acuityFemaleYesYesSecond cousin of 204100.6.1; Sister of 204100.6.3
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