210370.3.3

Country

Lebanon

HPO Terms

Blindness; Chorioretinal atrophy
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_207352.3:c.332T>C2

Remarks

Son of 210370.3.1 (F3:V-3)

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
210370.3.1LebanonBlindness; Chorioretinal atrophyFemaleYesNoF3:IV-7
210370.3.2LebanonBlindness; Chorioretinal atrophyFemaleYesYesDaughter of 210370.3.1 (F3:V-2)
210370.3.4LebanonNyctalopia; Choriocapillaris atrophy; Retinal pigment epithelial atrophy; Paracentral scotoma; Retinal crystalsFemaleYesYesDaughter of 210370.3.1 (F3:V-8)
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