272800.6.1

Country

Morocco

HPO Terms

Global developmental delay; Cherry red spot of the macula; Paralysis
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Sex

Female

Family History

No

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_000520.5:c.910_912delTTC1
NM_000520.5:c.540C>G1

Remarks

Moroccan Jew; Compound heterozygous

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
272800.6.2MoroccoMaleYesFather of 272800.6.1
272800.6.3MoroccoFemaleYesMother of 272800.6.1
272800.6.4MoroccoUnknownYesFirst degree cousin of 272800.6.1
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