610188.5

Country

Saudi Arabia

HPO Terms

Generalized hypotonia; Global developmental delay; Visual impairment; Nystagmus
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Sex

Female

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_025114.4:c.4714G>T2NA

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
610188.4Saudi ArabiaGlobal developmental delay; Intellectual disability; Seizure; Abnormal posterior cranial fossa morphologyFemaleYesYesAffected sibling
610188.6Saudi ArabiaRetinal dystrophy; Nephronophthisis; Molar tooth sign on MRIFemaleYes
610188.7Saudi ArabiaGlobal developmental delay; Molar tooth sign on MRIFemaleYesYes
610188.8Saudi ArabiaGlobal developmental delay; Molar tooth sign on MRIFemaleYesYes
610188.9Saudi ArabiaMolar tooth sign on MRIUnknown
610188.10Saudi ArabiaMolar tooth sign on MRI; NephronophthisisUnknown
610188.11Saudi ArabiaAtaxia; Molar tooth sign on MRI; Global developmental delay; HypotoniaUnknownYesPatient from 'JS_F11' family in the publication
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