DISEASES

Disease-gene associations mined from literature

Human genes for Seckel syndrome

Seckel syndrome [DOID:0050569]

A dysostosis that results_in abnormal development located_in vertebrae or located_in ribs. The bones of the spine do not develop properly, which causes them to be misshapen and abnormally joined together.

Synonyms:  Seckel syndrome,  DOID:0050569,  Seckel disease,  Seckel disorder,  bird-headed dwarfism ...

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7 #8 #9