Search Ontology:
Human Disease

autosomal recessive intellectual developmental disorder 68

Term ID
DOID:0081229
Synonyms
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the TRMT1 gene on chromosome 19p13. https://pubmed.ncbi.nlm.nih.gov/30289604/
References
Ontology
Human Disease   ( DOID:0081229 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models