autosomal recessive intellectual developmental disorder 39

Term ID

DOID:0081204

Synonyms

Definition

An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the TTI2 gene on chromosome 8p12. https://pubmed.ncbi.nlm.nih.gov/23956177/

References

• OMIM:615541

Ontology

Human Disease   ( DOID:0081204 )