Glutamate pyruvate transaminase 2 deficiency
MONDO:0014567Also known as: GPT2 Deficiency, GPT2 deficiency, glutamate pyruvate transaminase 2 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
2 clinical trials for this condition and its sub-types, 0 tagged with Glutamate pyruvate transaminase 2 deficiency itself.
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