204100.7.4

Country

Tunisia

HPO Terms

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

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

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

Remarks

Sister of 204100.7.1

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
204100.7.1TunisiaRetinal dystrophy; Progressive visual loss; Congenital stationary night blindness; Congenital nystagmus; Severely reduced visual acuityMaleYesYes
204100.7.2TunisiaRetinal dystrophy; Progressive visual loss; Congenital stationary night blindness; Congenital nystagmus; Severely reduced visual acuityMaleYesYesBrother of 204100.7.1
204100.7.3TunisiaRetinal dystrophy; Progressive visual loss; Congenital stationary night blindness; Congenital nystagmus; Severely reduced visual acuityMaleYesYesBrother of 204100.7.1
204100.7.5TunisiaRetinal dystrophy; Progressive visual loss; Congenital stationary night blindness; Congenital nystagmus; Severely reduced visual acuityMaleYesYesNiece of 204100.7.1
204100.7.6TunisiaHigh myopia; Age-related cataract; Diabetes mellitusMother of 204100.7.1
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