609180.1.2

Country

Yemen

HPO Terms

Global developmental delay; Hypotonia; Strabismus; Visual impairment; Hypopigmentation of the fundus; Scaling skin; Dry skin; Eczema; Brain atrophy
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_004870.3:c.310G>A2

Remarks

Brother of 609180.1.1

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
609180.1.1YemenCongenital hypothyroidism; Congenital adrenal hyperplasia; Seizure; Global developmental delay; Hypotonia; Strabismus; Lichenification; Brain atrophy; Dilated cardiomyopathy; Patent ductus arteriosusFemaleYesYes
609180.1.3YemenMaleFather of 609180.1.1
609180.1.4YemenFemaleMother of 609180.1.1
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