1 Matching Annotations
  1. Jul 2024
    1. Case: patient from family 1, male

      Disease Assertion: UCD/OTCD

      Family Info: Family history of the disease

      Case Presenting HPOs: coma(HP:0001259), lethargy(HP:0001254), hyperammonemia (HP:0001987), Neonatal Onset HP:0003623

      Case HPO FreeText: Poor feeding, poor spirit

      Case NOT HPOs:

      Case NOT HPO Free Text:

      Case Previous Testing: Genomic DNA was extracted using the QIAamp DNA Blood Midi Kit (Qiagen, Duesseldorf, Germany). Quality control assessment of DNA samples was performed using the NanoDrop 2000 ultra-microvolume nucleic acid and protein spectrophotometer (Thermo, Waltham, MA, USA). The purity of DNA was required to be between 1.8 and 2.0.

      Supplemental Data: TABLE 1, admitted to neonatal department because of poor feeding, poor spirit, coma, and lethargy. The maternal grandmother of the proband in this family had given birth to 3 boys and 2 girls. Two boys died within 1 month after birth

      Variant: NM_000531.6: c.867+1G>C

      ClinVarID:N/A

      CAID: CA412723994

      gnomAD:

      Gene Name: OTC (ornithine transcarbamylase)