A monogenic disease that has material basis in mutation in the FOXG1 gene.

Synonyms: inherited genetic disease caused by mutation in FOXG1 FOXG1 disorder FOXG1 inherited genetic disease

This is just here as a test because I lose it

Term information

Subsets

rare, nord_rare, clingen

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/5588

comment

Subtypes of the heterogeneous, eponymously named Congenital variant of Rett Syndrome, and Atypical Rett Syndrome are caused by mutations in the gene FOXG1. The common and most penetrant phenotype shared among these disease entities is neurodevelopmental impairment present in early infancy, progressive microcephaly, and MRI of the brain showing reduced myelinization and/or abnormal corpus callosum. Stereotypic hand movements, epilepsy, and abnormal breathing can have variable phenotypic expressivity.

creator

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

date

2018-06-29T19:29:48Z

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0015653

http://purl.obolibrary.org/obo/MONDO_0000508

id

MONDO:0100040

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0100040