301040.1.3

Country

Yemen

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_000489.6:c.5666T>G1

Remarks

Mother of 301040.1.1; X-Chromosome with mutation found to be preferentially activated (80%)

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
301040.1.1YemenGlobal developmental delay; Delayed speech and language development; Finger clinodactyly; Cerebral cortical atrophy; Abnormal facial shapeMaleYesYes
301040.1.2YemenGlobal developmental delay; Delayed speech and language development; Cerebral cortical atrophy; Abnormal facial shapeMaleYesYesSibling of 301040.1.1
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