612921.1.1

Country

Oman

HPO Terms

Intrauterine growth retardation; Short stature; Macrocephaly; Abnormal facial shape; Clinodactyly
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_015311.3:c.1119G>C2

Remarks

Emirati family of omani origin. Six affected children

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
612921.1.2OmanIntrauterine growth retardation; Short stature; Macrocephaly; Abnormal facial shape; ClinodactylyMaleYesYesSibling of 612921.1.1
612921.1.3OmanIntrauterine growth retardation; Short stature; Macrocephaly; Abnormal facial shape; ClinodactylyFemaleYesYesSibling of 612921.1.1
612921.1.4OmanMaleFather of 612921.1.1
612921.1.5OmanFemaleMother of 612921.1.1
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