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Human Disease

autosomal dominant intellectual developmental disorder 63 with macrocephaly

Term ID
DOID:0061036
Synonyms
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the TRIO gene on chromosome 5p15. https://pubmed.ncbi.nlm.nih.gov/32109419/
References
Ontology
Human Disease   ( DOID:0061036 )
Relationships
is a type of
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Genes Involved
Zebrafish Models