| Term Name: | autosomal recessive intellectual developmental disorder 51 |
|---|---|
| Synonyms: | |
| Definition: | An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the HNMT gene on chromosome 2q22. |
| Ontology: | Human Disease [DOID:0081214] ( DOID:0081214 ) |