600151.1.1

Country

Lebanon

HPO Terms

Rod-cone dystrophy; Truncal obesity; Global developmental delay; Hypodontia; Cataract; Brachydactyly; Syndactyly; Clinodactyly; Hepatic fibrosis; Postural instability
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_032146.5:c.68T>C2

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
600151.1.2LebanonRod-cone dystrophy; Truncal obesity; Global developmental delay; Polydactyly; Astigmatism; Brachydactyly; Syndactyly; Clinodactyly; Postural instabilityFemaleYesYesSister of 600151.1.1
600151.1.3LebanonFemaleMother of 600151.1.1
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