autosomal recessive intellectual developmental disorder 37

Term ID

DOID:0081202

Synonyms

Definition

An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the ANK3 gene on chromosome 10q21. https://pubmed.ncbi.nlm.nih.gov/29302074/

References

• OMIM:615493

Ontology

Human Disease   ( DOID:0081202 )