Term Name: | neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies |
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Synonyms: | autosomal recessive mental retardation 36 |
Definition: | An autosomal recessive intellectual developmental disorder that is characterized by global developmental delay with delayed walking, impaired intellectual development, and speech delay apparent from infancy or early childhood and that has_material_basis_in homozygous mutation in the ADAT3 gene on chromosome 19p13. |
Ontology: | Human Disease [DOID:0081099] ( DOID:0081099 ) |