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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

    0 descendants.

    Expanded Value Set

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