| Label | Id | |
|---|---|---|
| MRT49 | 14567 | |
| GPT2 deficiency | 14567 | |
| postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome | 14567 | |
| mental retardation, autosomal recessive 49 | 14567 | |
| mental retardation, autosomal recessive 49; MRT49 | http://purl.obolibrary.org/obo/MONDO_0014567 | |
| mental retardation, autosomal recessive type 49 | 14567 | |
| glutamate pyruvate transaminase 2 deficiency | 14567 |