familial amyotrophic lateral sclerosis
Go to external page http://purl.obolibrary.org/obo/MONDO_0005144
An instance of amyotrophic lateral sclerosis that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]
Synonyms: hereditary amyotrophic lateral sclerosis
This is just here as a test because I lose it
Term information
database
cross reference
- OMIMPS:105400 (MONDO:equivalentTo)
- EFO:0001356 (MONDO:equivalentTo)
- MEDGEN:1642547 (MONDO:equivalentTo)
- UMLS:C4551993 (MONDO:equivalentTo)
Subsets
gard_rare, otar, rare, nord_rare, clingen
exactMatch
http://identifiers.org/medgen/1642547
http://linkedlifedata.com/resource/umls/id/C4551993
https://omim.org/phenotypicSeries/PS105400