Search Ontology:
Human Disease
autosomal recessive intellectual developmental disorder 75
- Term ID
- DOID:0081234
- Synonyms
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- Definition
- An autosomal recessive intellectual developmental disorder that is characterized by global developmental delay apparent from infancy or early childhood and moderate to profoundly impaired intellectual development and that has_material_basis_in homozygous mutation in the PIDD1 gene on chromosome 11p15. https://pubmed.ncbi.nlm.nih.gov/34163010/
- References
- Ontology
- Human Disease ( DOID:0081234 )
- is a type of
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Genes Involved
Zebrafish Models