Male
Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
---|---|---|---|---|
NM_000071.3:c.457G>A | 1 | NA |
Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
---|---|---|---|---|---|---|
236200.15.1 | Saudi Arabia | Intellectual disability; Hyperhomocystinemia; Hypermethioninemia; Lens subluxation; Scoliosis; Osteoporosis; Peripheral neuropathy; Attention deficit hyperactivity disorder; Varicose veins; Vascular tortuosity; Abnormal nerve conduction velocity | Male | Yes | Yes | Patient II-1 from Family 13 in the publication |
236200.15.2 | Saudi Arabia | Intellectual disability; Hyperhomocystinemia; Hypermethioninemia; Lens subluxation; Attention deficit hyperactivity disorder; Precocious puberty | Male | Yes | Yes | Patient II-3 from Family 13 in the publication, brother of 236200.15.1 |
236200.15.4 | Saudi Arabia | Female | Mother of 236200.15.1 |