300604.1.1

Country

Lebanon

HPO Terms

Tall stature; Primary amenorrhea; Delayed puberty; Osteoporosis; Fragile teeth
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Sex

Female

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001324036.2:c.139T>C2

Remarks

Multiply consanguineous family, with multiple members affected by albinism, FMF, Behcet and/or retinitis pigmentosa

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
300604.1.2LebanonPrimary amenorrhea; Delayed puberty; Osteoporosis; Fragile teethFemaleYesYesSister of 300604.1.1
300604.1.3LebanonPrimary amenorrhea; Delayed puberty;FemaleYesYesSister of 300604.1.1
300604.1.4LebanonPrimary amenorrhea; Delayed puberty;FemaleYesYesSister of 300604.1.1
300604.1.5LebanonPrimary amenorrhea; Delayed puberty;FemaleYesYesSister of 300604.1.1
300604.1.6LebanonFemaleYesSister of 300604.1.1
300604.1.7LebanonFemaleMother of 300604.1.1
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