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Human Disease

neurodevelopmental disorder with poor growth and behavioral abnormalities

Term ID
DOID:0081444
Synonyms
Definition
An autosomal recessive intellectual developmental disorder that is characterized by global developmental delay, moderately to severely impaired intellectual development, often with absent speech, and behavioral abnormalities, including hyperactivity, short attention span, and ADHD and that has_material_basis_in homozygous or compound heterozygous mutation in the ATP9A gene on chromosome 20q13. (2)
References
Ontology
Human Disease   ( DOID:0081444 )
Relationships
is a type of
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Genes Involved
Zebrafish Models