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Resources » Disease Ontology

chromosome 15q26-qter deletion syndrome

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  • Overview

    chromosome 15q26-qter deletion syndrome

    Ontology Term:
    Status:
    Live
    Synonym:
    15q26 deletion syndrome
    Drayer syndrome
    distal 15q deletion syndrome
    distal monosomy 15q
    telomeric 15q deletion syndrome
    Type:
    Mapping to OMIM ID:
    Comparative Info:
    Learn more about this disease from studies in other model systems at the
    WormBase ID:
    DOID:0060397
    A chromosomal deletion syndrome that is characterized by pre- and postnatal growth restriction, developmental delay, variable degrees of intellectual disability, brachy-clinodactyly, talipes equinovarus, nail hypoplasia, proximally placed digits and mild craniofacial dysmorphism including microcephaly, triangular face, broad nasal bridge and micrognathia.
    Child:
    Associations based on experimental data:
    Disease relevant gene:
    Automatic gene association:
    1 Inferred automatically: Inferred by orthology to human genes with OMIM annotation