All diseases

OMIM ID
162100
OMIM term:
AMYOTROPHY, HEREDITARY NEURALGIC; HNA
Alternative terms:
NEURITIS WITH BRACHIAL PREDILECTION; NAPB
BRACHIAL PLEXUS NEUROPATHY, HEREDITARY
AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS
(∗) Location:
17q25.2-q25.3  
(†) Associated OMIM genes:
SEPT9  
(‡) Associated MGI genes:

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