All diseases

OMIM ID
613115
OMIM term:
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B
Alternative terms:

(∗) Location:
5p15.1  
(†) Associated OMIM genes:
FAM134B  
(‡) Associated MGI genes:

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