A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles. [ https://orcid.org/0000-0002-0736-9199 ]

Synonyms: neurogenetic disease

This is just here as a test because I lose it

Term information

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/5952

creator

https://orcid.org/0000-0001-5208-3432

id

MONDO:0100545

Term relations