All diseases

OMIM ID
270710
OMIM term:
FITZSIMMONS-GUILBERT SYNDROME
Alternative terms:
SPASTIC PARAPLEGIA ASSOCIATED WITH BRACHYDACTYLY TYPE E
FITZSIMMONS SYNDROME
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/mhjmtldv