Disease

neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies

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.

Synonyms

autosomal recessive mental retardation 36

Cross References

MIM:615286

Parent Terms

autosomal recessive intellectual developmental disorder

Child Terms

None

Sources of Associations

Associated Genes

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Associated Alleles

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Associated Models

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