OBO ID: DOID:0081229
Term Name: autosomal recessive intellectual developmental disorder 68 Search Ontology:
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 )
OTHER autosomal recessive intellectual developmental disorder 68 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TRMT1 Intellectual developmental disorder, autosomal recessive 68 618302
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None