Disease #01464 (amyotrophy, neuralgic, hereditary, OMIM:162100)

Official abbreviation -
Name amyotrophy, neuralgic, hereditary
OMIM ID 162100
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SEPT9
Associated tissues -
Disease features -
Remarks -