Submission Details

Submitter:

Classification:
Definitive
GENCC:100001
Gene:
Disease:
osteogenesis imperfecta type 2
OMIM:166210
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
09/01/2017
PubMed IDs:
21834035 8364588 2037280 3403550 2794057 8950680 8097422 7816518 3667599 8100209 12538651 1613761 2298750 3108247 1864604 7881420 2309707 2500431 2913053 1874719 2339700
Assertion Criteria:
Submitter Submitted Date:
09/11/2023

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