158350.2

Country

United Arab Emirates

HPO Terms

Hyperpigmentation of the skin; Macrocephaly; Abnormal facial shape
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Sex

Male

Family History

No

Parental Consanguinity

No

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_000314.6:c.70G>C1

Remarks

de novo mutation

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
158350.1United Arab EmiratesGlobal developmental delay; MacrocephalyMaleNoYesde novo mutation
158350.3United Arab EmiratesMacrocephaly; Delayed speech and language development; Arachnoid cyst; Hamartoma; Lipoma; Gait disturbanceFemaleNoYesde novo mutation
158350.4United Arab EmiratesMicrocephaly; Intellectual disability; Seizure; Cerebral atrophy; Scoliosis; Hip dislocation; Hyperpigmentation of the skinMaleYesNo
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