Search Ontology:
Human Disease
autosomal recessive intellectual developmental disorder 70
- Term ID
- DOID:0081231
- Synonyms
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- Definition
- An autosomal recessive intellectual developmental disorder that is characterized primarily by impaired intellectual developmen and that has_material_basis_in homozygous mutation in the RSRC1 gene on chromosome 3q25. https://pubmed.ncbi.nlm.nih.gov/28640246/
- References
- Ontology
- Human Disease ( DOID:0081231 )
- is a type of
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Genes Involved
Zebrafish Models