136880.2

Country

Saudi Arabia

HPO Terms

Retinal dystrophy; Seizure; Fundus albipunctatus
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Sex

Unknown

Family History

No

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_000326.5:c.773T>G2

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
136880.1Saudi ArabiaRod-cone dystrophyUnknownNo
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