Search Ontology:
Human Disease
autosomal recessive intellectual developmental disorder 51
- Term ID
- DOID:0081214
- Synonyms
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- Definition
- An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the HNMT gene on chromosome 2q22. https://pubmed.ncbi.nlm.nih.gov/26206890/
- References
- Ontology
- Human Disease ( DOID:0081214 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models