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52171000: Ocular albinism-lentigines-deafness syndrome (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    86830019 Ocular albinism-lentigines-deafness syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
    790151017 Ocular albinism-lentigines-deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Ocular albinism-lentigines-deafness syndrome Is a Hypopigmentation of skin false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Is a Lentigo false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Is a Ocular albinism false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Associated morphology Hyperpigmentation false Inferred relationship Existential restriction modifier 1
    Ocular albinism-lentigines-deafness syndrome Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 3
    Ocular albinism-lentigines-deafness syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Ocular albinism-lentigines-deafness syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 3
    Ocular albinism-lentigines-deafness syndrome Finding site Structure of nervous system false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Pathological process Benign neoplastic process false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Associated morphology Pigmented nevus, no International Classification of Diseases for Oncology subtype false Inferred relationship Existential restriction modifier 3
    Ocular albinism-lentigines-deafness syndrome Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 1
    Ocular albinism-lentigines-deafness syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Ocular albinism-lentigines-deafness syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Finding site Orbital region structure false Inferred relationship Existential restriction modifier 1
    Ocular albinism-lentigines-deafness syndrome Finding site Structure of skin region false Inferred relationship Existential restriction modifier 2
    Ocular albinism-lentigines-deafness syndrome Is a Neoplasm of eye region false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Is a Benign tumor of head and neck false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Ocular albinism-lentigines-deafness syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 3
    Ocular albinism-lentigines-deafness syndrome Is a Benign neoplasm of skin false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Finding site Structure of skin region false Inferred relationship Existential restriction modifier 3
    Ocular albinism-lentigines-deafness syndrome Finding site Structure of skin region false Inferred relationship Existential restriction modifier 5
    Ocular albinism-lentigines-deafness syndrome Finding site Structure of skin region false Inferred relationship Existential restriction modifier 2
    Ocular albinism-lentigines-deafness syndrome Is a Melanocytic tumor of skin false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Is a Melanocytic nevus of skin false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Is a Acquired melanocytic nevus false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Is a Lentigo false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Ocular albinism-lentigines-deafness syndrome Finding site Structure of skin region false Inferred relationship Existential restriction modifier 3
    Ocular albinism-lentigines-deafness syndrome Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
    Ocular albinism-lentigines-deafness syndrome Associated morphology Structure showing abnormal deposition of pigment false Inferred relationship Existential restriction modifier 2
    Ocular albinism-lentigines-deafness syndrome Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 1
    Ocular albinism-lentigines-deafness syndrome Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier 2
    Ocular albinism-lentigines-deafness syndrome Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 1
    Ocular albinism-lentigines-deafness syndrome Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
    Ocular albinism-lentigines-deafness syndrome Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier 2
    Ocular albinism-lentigines-deafness syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Ocular albinism-lentigines-deafness syndrome Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 1
    Ocular albinism-lentigines-deafness syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
    Ocular albinism-lentigines-deafness syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
    Ocular albinism-lentigines-deafness syndrome Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 3
    Ocular albinism-lentigines-deafness syndrome Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 4
    Ocular albinism-lentigines-deafness syndrome Is a Genetic disorder of skin pigmentation false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Associated morphology Lentigo false Inferred relationship Existential restriction modifier 2
    Ocular albinism-lentigines-deafness syndrome Is a Lentiginosis false Inferred relationship Existential restriction modifier
    Ocular albinism-lentigines-deafness syndrome Finding site Structure of skin and/or mucous membrane false Inferred relationship Existential restriction modifier 2
    Ocular albinism-lentigines-deafness syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Ocular albinism-lentigines-deafness syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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