236200.15.2

Country

Saudi Arabia

HPO Terms

Intellectual disability; Hyperhomocystinemia; Hypermethioninemia; Lens subluxation; Attention deficit hyperactivity disorder; Precocious puberty
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_000071.3:c.457G>A2NA

Remarks

Patient II-3 from Family 13 in the publication, brother of 236200.15.1

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
236200.15.1Saudi ArabiaIntellectual disability; Hyperhomocystinemia; Hypermethioninemia; Lens subluxation; Scoliosis; Osteoporosis; Peripheral neuropathy; Attention deficit hyperactivity disorder; Varicose veins; Vascular tortuosity; Abnormal nerve conduction velocityMaleYesYesPatient II-1 from Family 13 in the publication
236200.15.3Saudi ArabiaMaleFather of 236200.15.1
236200.15.4Saudi ArabiaFemaleMother of 236200.15.1
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