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Resources » Disease Ontology

autosomal recessive intellectual developmental disorder 27

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  • Overview

    autosomal recessive intellectual developmental disorder 27

    Ontology Term:
    Status:
    Live
    Synonym:
    Type:
    Mapping to OMIM ID:
    Comparative Info:
    Learn more about this disease from studies in other model systems at the
    WormBase ID:
    DOID:0081193
    An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the LINS gene (LINS1) on chromosome 15q26.
    Child:
    Associations based on experimental data:
    Disease relevant gene:
    Automatic gene association:
    1 Inferred automatically: Inferred by orthology to human genes with OMIM annotation