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610915.6
Home
Subject Details
Country
Oman
HPO Terms
Recurrent infections
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Sex
Male
Family History
Yes
Parental Consanguinity
Yes
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
NM_022356.4:c.2056-1G>A
2
NA
Osteogenesis Imperfecta, Type VIII
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References
Maddirevula et al. 2018
Related Subjects
Subject Id
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Sex
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Parental Consanguinity
610915.1
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610915.7
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Osteopenia; Pulmonary hypoplasia; Recurrent fractures
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Yes
Yes
Back to search Result
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العربية
About Us
News
Fellowships
العربية
Home
About Us
CTGA Database
CTGA Overview
Search Database
Submit to Database
Publications
Research Articles
Genetics Made Easy
Genetic Disorders in the Arab World
Reports
Conferences & Events
News
Gallery
Fellowships
Contact Us
