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721905000: Robinow-like syndrome (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    3326815014 Robinow-like syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3326816010 Robinow-like syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3326817018 The association of the clinical features present in Robinow syndrome (short stature, mesomelic brachymelia, macrocephaly and hypoplastic genitalia) with anterior chamber cleavage anomalies. It has been described in two sisters and is transmitted as an autosomal recessive trait. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3326815014 Robinow-like syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3326816010 Robinow-like syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3326817018 The association of the clinical features present in Robinow syndrome (short stature, mesomelic brachymelia, macrocephaly and hypoplastic genitalia) with anterior chamber cleavage anomalies. It has been described in two sisters and is transmitted as an autosomal recessive trait. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Robinow-like syndrome Is a Congenital anomaly of anterior chamber of eye false Inferred relationship Existential restriction modifier (core metadata concept)
    Robinow-like syndrome Is a Multiple malformation syndrome, moderate short stature, facial false Inferred relationship Existential restriction modifier (core metadata concept)
    Robinow-like syndrome Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    Robinow-like syndrome Is a Mesomelic dysplasia false Inferred relationship Existential restriction modifier (core metadata concept)
    Robinow-like syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    Robinow-like syndrome Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
    Robinow-like syndrome Is a Hereditary disorder of the visual system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Robinow-like syndrome Is a Congenital anomaly of face (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Robinow-like syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Robinow-like syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Robinow-like syndrome Finding site Anterior chamber of eye structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Robinow-like syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
    Robinow-like syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 6
    Robinow-like syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 5
    Robinow-like syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 5
    Robinow-like syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 6
    Robinow-like syndrome Finding site Face structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 6
    Robinow-like syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Robinow-like syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Robinow-like syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Robinow-like syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Robinow-like syndrome Finding site Anterior chamber of eye structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Robinow-like syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Robinow-like syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Robinow-like syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Robinow-like syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Robinow-like syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Robinow-like syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Robinow-like syndrome Finding site Face structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    REPLACED BY association reference set (foundation metadata concept)

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