265000.3.2

Country

Lebanon

HPO Terms

Decreased fetal movement; Arthrogryposis multiplex congenita; Pterygium; Short stature; Kyphosis; Scoliosis; Abnormal facial shape; High palate; Arachnodactyly; Cryptorchidism
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_005199.5:c.807dup2

Remarks

Brother of 265000.3.1

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
265000.3.1LebanonArthrogryposis multiplex congenita; Pterygium; Short stature; Kyphosis; Scoliosis; Abnormal facial shape; High palate; ArachnodactylyFemaleYesYesProband
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