619055.7.2

Country

Lebanon
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Sex

Male

Family History

No

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001171155.2:c.3G>C1

Remarks

Unaffected father of 619055.7.1

References

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
619055.7.1LebanonGlobal developmental delay; Hypotonia; Seizure; Increased CSF lactate; Increased serum lactate; Cerebral cortical atrophy; Death in infancyFemaleNoYes
619055.7.3LebanonFemaleNoUnaffected mother of 619055.7.1
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