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83386001: Congenital hypopigmentation (morphologic abnormality)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    138307014 Congenital hypopigmentation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    825008010 Congenital hypopigmentation (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    138307014 Congenital hypopigmentation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    138307014 Congenital hypopigmentation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    825008010 Congenital hypopigmentation (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    825008010 Congenital hypopigmentation (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital hypopigmentation Is a Congenital pigmentation false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital hypopigmentation Is a Hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Minimal pigment oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Temperature-sensitive oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Tyrosinase-positive oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ocular albinism-lentigines-deafness syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 3
    albinoïdisme Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Waardenburg syndrome type 3 (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Punctate oculocutaneous albinoidism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Rufous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Tyrosinase-negative oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Autosomal recessive ocular albinism (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 3
    Autosomal dominant oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Yellow mutant oculocutaneous albinism (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hermansky-Pudlak syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Aland eye disease and ocular albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital deficiency of pigment of skin Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ocular albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hypopigmentation-immunodeficiency disease Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 3
    Congenital oculocutaneous hypopigmentation Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Partial albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Woolf's syndrome (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Ocular albinism, type I Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital hypopigmentation of choroid (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Black locks, oculocutaneous albinism, AND deafness of the sensorineural type Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Chédiak-Higashi syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)
    Brown oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Oculocutaneous albinoidism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Cross syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 3
    Albinism-deafness syndrome of Tietz (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)
    Ziprkowski-Margolis syndrome (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)
    Phylloid hypomelanosis Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)
    Aland eye disease and ocular albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Temperature-sensitive oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Partial albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)
    Minimal pigment oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ocular albinism, type I Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Tyrosinase-positive oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ziprkowski-Margolis syndrome (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Cross syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 3
    Albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)
    Rufous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Oculocutaneous albinoidism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Ocular albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Punctate oculocutaneous albinoidism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Albinism-deafness syndrome of Tietz (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Waardenburg syndrome type 3 (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Chédiak-Higashi syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hermansky-Pudlak syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Autosomal dominant oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Black locks, oculocutaneous albinism, AND deafness of the sensorineural type Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Autosomal recessive ocular albinism (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Brown oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hypopigmentation-immunodeficiency disease Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)
    Tyrosinase-negative oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Woolf's syndrome (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)
    albinoïdisme Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Yellow mutant oculocutaneous albinism (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Phylloid hypomelanosis Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ocular albinism-lentigines-deafness syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital oculocutaneous hypopigmentation Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ocular albinism-lentigines-deafness syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Tyrosinase-positive oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hermansky-Pudlak syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Black locks, oculocutaneous albinism, AND deafness of the sensorineural type Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ocular albinism, type I Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    albinoïdisme Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Brown oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Autosomal dominant oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Minimal pigment oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Rufous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ocular albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Yellow mutant oculocutaneous albinism (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Oculocutaneous albinoidism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital hypopigmentation of choroid (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Tyrosinase-negative oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Punctate oculocutaneous albinoidism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Autosomal recessive ocular albinism (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Aland eye disease and ocular albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital deficiency of pigment of skin Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Temperature-sensitive oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    albinoïdisme Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Brown oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Rufous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Partial albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Albinism-deafness syndrome of Tietz (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Minimal pigment oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Yellow mutant oculocutaneous albinism (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hermansky-Pudlak syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ziprkowski-Margolis syndrome (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Tyrosinase-positive oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Woolf's syndrome (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 1
    Albinotic fundus (disorder) Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 3
    Autosomal dominant oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital deficiency of pigment of skin Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Tyrosinase-negative oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Temperature-sensitive oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 2
    Cross syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept) 6

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    Reference Sets

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

    SAME AS association reference set (foundation metadata concept)

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