Disease-gene associations mined from literature

Human genes for Alexander disease

Alexander disease [DOID:4252]

Alexander disease is a slowly progressing and fatal neurodegenerative disease. It is a very rare disorder which results from a genetic mutation and mostly affects infants and children, causing developmental delay and changes in physical characteristics.

Synonyms:  Alexander disease,  Alexander disorder,  Alexander syndrome,  DOID:4252,  Alexander's disease ...

Linkouts:  OMIM