Disease - Intellectual developmental disorder, autosomal recessive 67
- DefinitionA form of intellectual disability, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. Some MRT67 patients manifest seizures and sensorineural hearing loss.
- AcronymMRT67
- Keywords
- Cross references
Disclaimer
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. Our staff consists of biologists and biochemists that are not trained to give medical advice.Related UniProtKB entry
Browse 1 entry- Eukaryotic translation initiation factor 3 subunit F · Gene: EIF3F (EIF3S5) · Homo sapiens (Human) · 357 amino acids · Evidence at protein level · Annotation score: 5/5