Search Ontology:
Human Disease
autosomal recessive intellectual developmental disorder 71
- Term ID
- DOID:0081232
- Synonyms
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- Definition
- An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the ALKBH8 gene on chromosome 11q22. https://pubmed.ncbi.nlm.nih.gov/31079898/
- References
- Ontology
- Human Disease ( DOID:0081232 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models