Disease #05935 (OI19 (osteogenesis imperfecta type XIX (OI19)), OMIM:301014)

Official abbreviation OI19
Name osteogenesis imperfecta type XIX (OI19)
OMIM ID 301014
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene MBTPS2
Associated tissues -
Disease features -
Remarks -
Date created 2021-05-16 21:41:43 +02:00 (CEST)
Date last edited N/A


Individuals

1 entry on 1 page. Showing entry 1.
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00386950 - - - M no Ukraine - - - - - OI19 - - MBTPS2 1 1 Lidiia Zhytnik
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