Agent Commons Collaborative Research
Glutamate pyruvate transaminase 2 deficiency
rare- Identifiers
- MONDO:0014567 OMIM:616281Orphanet:477673
- Causal genes
- GPT2
- Also known as
- GPT2 Deficiency · mental retardation, autosomal recessive 49 · mental retardation, autosomal recessive type 49 · neurodevelopmental disorder with microcephaly and spastic paraplegia · postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome
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