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722111004: Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 30-Jun 2022. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    3330735017 Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    3330736016 Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Is a Sensorineural hearing loss false Inferred relationship Existential restriction modifier
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Is a Multiple malformation syndrome with facial defects as major feature false Inferred relationship Existential restriction modifier
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Is a Mental retardation false Inferred relationship Existential restriction modifier
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Is a Congenital hearing disorder false Inferred relationship Existential restriction modifier
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Is a Osteopenia false Inferred relationship Existential restriction modifier
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Is a Auditory system hereditary disorder false Inferred relationship Existential restriction modifier
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Is a Congenital connective tissue disorder false Inferred relationship Existential restriction modifier
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Finding site Structure of auditory system false Inferred relationship Existential restriction modifier 3
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Interprets Hearing, function false Inferred relationship Existential restriction modifier 4
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Interprets Functional observable false Inferred relationship Existential restriction modifier
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Associated morphology Osteopenia false Inferred relationship Existential restriction modifier 5
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 5
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 6
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 6
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 6
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Is a Intellectual disability false Inferred relationship Existential restriction modifier
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Is a Congenital anomaly of skeletal bone false Inferred relationship Existential restriction modifier
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 1
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Associated morphology Osteopenia false Inferred relationship Existential restriction modifier 2
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 2
    Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Is a Developmental hereditary disorder false Inferred relationship Existential restriction modifier

    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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