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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
    45881000052116 kongenital hypopigmentering sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    kongenital hypopigmentering Is a medfödd pigmentering false Inferred relationship Some
    kongenital hypopigmentering Is a Hypopigmentation false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Cross syndrome Associated morphology False kongenital hypopigmentering Inferred relationship Some 6
    Chédiak-Higashi syndrome Associated morphology False kongenital hypopigmentering Inferred relationship Some 1
    Oculocutaneous albinism Associated morphology False kongenital hypopigmentering Inferred relationship Some 2
    Phylloid hypomelanosis (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 1
    Punctate oculocutaneous albinoidism Associated morphology False kongenital hypopigmentering Inferred relationship Some 3
    okulokutan albinoidism Associated morphology False kongenital hypopigmentering Inferred relationship Some 3
    Aland eye disease and ocular albinism Associated morphology False kongenital hypopigmentering Inferred relationship Some 3
    Ocular albinism Associated morphology False kongenital hypopigmentering Inferred relationship Some 3
    Ocular albinism, type I Associated morphology False kongenital hypopigmentering Inferred relationship Some 3
    Autosomal recessive ocular albinism (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 3
    Hypopigmentation-immunodeficiency disease Associated morphology False kongenital hypopigmentering Inferred relationship Some 1
    okulär albinism - lentiginos - dövhetssyndrom Associated morphology False kongenital hypopigmentering Inferred relationship Some 3
    Black locks, oculocutaneous albinism, AND deafness of the sensorineural type Associated morphology False kongenital hypopigmentering Inferred relationship Some 2
    Congenital hypopigmentation of choroid Associated morphology False kongenital hypopigmentering Inferred relationship Some 3
    parodontit samtidigt med Chédiak-Higashis syndrom Associated morphology False kongenital hypopigmentering Inferred relationship Some 7
    Congenital oculocutaneous hypopigmentation Associated morphology False kongenital hypopigmentering Inferred relationship Some 3
    Albinism co-occurrent with hematologic disorder (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 4
    Oculocutaneous albinism type 4 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 4
    Oculocutaneous albinism type 4 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 6
    Oculocerebral hypopigmentation syndrome of Preus type (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 2
    Oculocerebral hypopigmentation syndrome of Preus type (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 3
    Piebaldism (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 1
    Microcephalus with albinism and digital anomaly syndrome (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 8
    Microcephalus with albinism and digital anomaly syndrome (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 11
    Congenital oculocutaneous hypopigmentation Associated morphology False kongenital hypopigmentering Inferred relationship Some 4
    Vici syndrome (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 8
    Vici syndrome (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 6
    Attenuated Chédiak-Higashi syndrome (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 4
    Deaf blind hypopigmentation syndrome Yemenite type (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 4
    Ocular albinism with late-onset sensorineural deafness (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 7
    Oculocutaneous albinism type 5 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 6
    Oculocutaneous albinism type 6 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 6
    Oculocutaneous albinism type 7 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 6
    Albinism with deafness syndrome (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 6
    Oculocutaneous albinism type 5 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 4
    Oculocutaneous albinism type 6 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 4
    Oculocutaneous albinism type 7 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 4
    Ocular albinism with late-onset sensorineural deafness (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 6
    Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 4
    Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 5
    Deafness, vitiligo, achalasia syndrome Associated morphology False kongenital hypopigmentering Inferred relationship Some 6
    Oculocutaneous albinism type 1 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 2
    Oculocutaneous albinism type 1 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 1
    Oculocutaneous albinism type 5 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 1
    Oculocutaneous albinism type 7 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 1
    Oculocutaneous albinism type 6 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 1
    Microcephalus with albinism and digital anomaly syndrome (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 4
    Oculocutaneous albinism type 4 (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 1
    Waardenburg's syndrome Associated morphology False kongenital hypopigmentering Inferred relationship Some 1
    Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 4
    Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder) Associated morphology False kongenital hypopigmentering Inferred relationship Some 3

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    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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