autosomal recessive intellectual developmental disorder 47

Term ID

DOID:0081211

Synonyms

Definition

An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the FMN2 gene on chromosome 1q43. https://pubmed.ncbi.nlm.nih.gov/25480035/

References

• OMIM:616193

Ontology

Human Disease   ( DOID:0081211 )