| Term Name: | autosomal recessive intellectual developmental disorder 47 |
|---|---|
| Synonyms: | |
| Definition: | An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the FMN2 gene on chromosome 1q43. |
| Ontology: | Human Disease [DOID:0081211] ( DOID:0081211 ) |