176200.1.1

Country

Lebanon

HPO Terms

Severe photosensitivity; Seizure; Neurodevelopmental delay; Increased fecal porphyrin
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Sex

Female

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_000309.5:c.1015G>A2

Remarks

Other affected relatives

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
176200.1.2LebanonSevere photosensitivity; Seizure; Neurodevelopmental delay; Increased fecal porphyrinMaleYesYesMaternal uncle of 176200.1.1
176200.1.3LebanonFemaleMother of 176200.1.1
176200.1.4LebanonMaleFather of 176200.1.1
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