All diseases

OMIM ID
200610
OMIM term:
ACHONDROGENESIS, TYPE II; ACG2
Alternative terms:
ACHONDROGENESIS, LANGER-SALDINO TYPE
CHONDROGENESIS IMPERFECTA
ACHONDROGENESIS, TYPE IB, FORMERLY HYPOCHONDROGENESIS, INCLUDED
(∗) Location:
12q13.11  
(†) Associated OMIM genes:
COL2A1  
(‡) Associated MGI genes:
Col2a1  

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