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Disease Ontology Browser
Antley-Bixler syndrome (DOID:0050462)
Alliance: disease page
Synonyms: trapezoidocephaly-synostosis syndrome
Alt IDs: OMIM:201750, OMIM:207410, MESH:D054882, UMLS_CUI:C1860042, UMLS_CUI:C2350233, UMLS_CUI:C2936791
Definition: An autosomal recessive disease that is characterized at birth or prenatally by malformations and deformities affecting the majority of the skeleton and other areas of the body with autosomal recessive inheritance of the FGFR2 gene.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory