Term info
database cross reference
- UMLS:CN207018 (MONDO:equivalentTo)
- Orphanet:98505 (MONDO:equivalentTo)
- SCTID:49793008 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
definition
An instance of motor neuron disease that is caused by an inherited modification of the individual's genome.
exactMatch
http://identifiers.org/snomedct/49793008, http://linkedlifedata.com/resource/umls/id/CN207018, http://purl.obolibrary.org/obo/Orphanet_98505
has exact synonym
genetic motor neuron disease, hereditary motor neuron disease, genetic anterior horn cell disease
id
MONDO:0024257