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83386001: Congenital hypopigmentation (morphologic abnormality)


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

    Descriptions:

    Id Description Lang Type Status Case? Module
    138307014 Congenital hypopigmentation en Synonym Active Entire term case insensitive SNOMED CT core module
    825008010 Congenital hypopigmentation (morphologic abnormality) 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
    Congenital hypopigmentation Is a Congenital pigmentation false Inferred relationship Existential restriction modifier
    Congenital hypopigmentation Is a Hypopigmentation false Inferred relationship Existential restriction modifier

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

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    This concept is not in any reference sets

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