210370.1.1

Country

Lebanon

HPO Terms

Nyctalopia; Choriocapillaris atrophy; Retinal pigment epithelial atrophy; Scotoma; Retinal crystals
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Sex

Female

Family History

Yes

Parental Consanguinity

No

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_207352.3:c.1372G>A2

Remarks

F1:II-1

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
210370.1.2LebanonNyctalopia; Choriocapillaris atrophy; Retinal pigment epithelial atrophy; Paracentral Scotoma; Retinal crystalsFemaleYesNoSister of 210370.1.1 (F1:II-2)
210370.1.3LebanonMaleNoNoFather of 210370.1.1
210370.1.4LebanonFemaleNoNoMother of 210370.1.1
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