Search Ontology:
Human Disease
autosomal recessive intellectual developmental disorder 66
- Term ID
- DOID:0081227
- Synonyms
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- Definition
- An autosomal recessive intellectual developmental disorder that is characterized by delayed speech development, neuropsychiatric symptoms, and relatively normal life span and that has_material_basis_in homozygous mutation in the C12ORF4 gene on chromosome 12p13. https://pubmed.ncbi.nlm.nih.gov/27311568/
- References
- Ontology
- Human Disease ( DOID:0081227 )
- is a type of
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Genes Involved
Zebrafish Models