236200.3.1

Country

Sudan

HPO Terms

Intellectual disability; Hyperhomocystinemia; Hypermethioninemia; Lens subluxation; Vascular tortuosity; Seizure
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_000071.3:c.770C>T2NA

Remarks

Patient IV-2 from Family 1 in the publication

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
236200.3.2SudanHyperhomocystinemiaFemaleYesYesPatient IV-3 from Family 1 in the publication, sister of 236200.3.1
236200.3.3SudanFemaleYesMother of 236200.3.1
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