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 0
Associated with 1 gene MBTPS2
Associated tissues -
Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00386950 - - - M no Ukraine - - - - - OI19 - - MBTPS2 1 1 Lidiia Zhytnik
Legend   How to query