608629.5

Country

Saudi Arabia

HPO Terms

Global developmental delay; Oculomotor apraxia; Hypotonia; Strabismus; Ataxia
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Sex

Male

Family History

No

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001134831.2:c.1328T>A2

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
608629.2Saudi ArabiaAtaxia; Intellectual disability; Global developmental delay; Molar tooth sign on MRIUnknownYesPatient from 'JS_A' family in the publication
608629.3Saudi ArabiaAtaxia; Intellectual disability; Global developmental delay; Molar tooth sign on MRIUnknownYesPatient from 'MTI-1501' family in the publication
608629.6Saudi ArabiaGlobal developmental delay; Oculomotor apraxia; Hypotonia; Strabismus; Ataxia; Abnormal facial shapeFemaleYesYesHas similarly affected sibling and cousin
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