613843.2.1

Country

Saudi Arabia

HPO Terms

Visual impairment; Nystagmus; Attenuation of retinal blood vessels; Hypermetropia; Dull foveal reflex; Depigmented fundus; Pigmentary retinopathy
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Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_003322.6:c.901C>T2

References

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
613843.2.2Saudi ArabiaMacular atrophy; Bone spicule pigmentation of the retina; NystagmusYesYesRelative of 613843.2.1
613843.2.3Saudi ArabiaNystagmus; Hypermetropia; Astigmatism; Optic disc pallor; Attenuation of retinal blood vessels; Bone spicule pigmentation of the retinaYesYesRelative of 613843.2.1
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