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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
    Cross syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 6
    Chédiak-Higashi syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 1
    Oculocutaneous albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 2
    Phylloid hypomelanosis Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 1
    Punctate oculocutaneous albinoidism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 3
    Oculocutaneous albinoidism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 3
    Aland eye disease and ocular albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 3
    Ocular albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 3
    Ocular albinism, type I Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 3
    Autosomal recessive ocular albinism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 3
    Hypopigmentation-immunodeficiency disease 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
    Black locks, oculocutaneous albinism, AND deafness of the sensorineural type Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 2
    Congenital hypopigmentation of choroid Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 3
    Periodontitis co-occurrent with Chédiak-Higashi syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 7
    Congenital oculocutaneous hypopigmentation Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 3
    Albinism co-occurrent with hematologic disorder Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 4
    Oculocutaneous albinism type 4 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 4
    Oculocutaneous albinism type 4 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 6
    Oculocerebral hypopigmentation syndrome of Preus type Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 2
    Oculocerebral hypopigmentation syndrome of Preus type Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 3
    Piebaldism Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 1
    Microcephalus with albinism and digital anomaly syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 8
    Microcephalus with albinism and digital anomaly syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 11
    Congenital oculocutaneous hypopigmentation Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 4
    Vici syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 8
    Vici syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 6
    Attenuated Chédiak-Higashi syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 4
    Deaf blind hypopigmentation syndrome Yemenite type Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 4
    Ocular albinism with late-onset sensorineural deafness Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 7
    Oculocutaneous albinism type 5 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 6
    Oculocutaneous albinism type 6 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 6
    Oculocutaneous albinism type 7 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 6
    Albinism with deafness syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 6
    Oculocutaneous albinism type 5 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 4
    Oculocutaneous albinism type 6 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 4
    Oculocutaneous albinism type 7 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 4
    Ocular albinism with late-onset sensorineural deafness Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 6
    Osteoporosis and oculocutaneous hypopigmentation syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 4
    Osteoporosis and oculocutaneous hypopigmentation syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 5
    Deafness, vitiligo, achalasia syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 6
    Oculocutaneous albinism type 1 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 2
    Oculocutaneous albinism type 1 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 1
    Oculocutaneous albinism type 5 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 1
    Oculocutaneous albinism type 7 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 1
    Oculocutaneous albinism type 6 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 1
    Microcephalus with albinism and digital anomaly syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 4
    Oculocutaneous albinism type 4 Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 1
    Waardenburg syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 1
    Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 4
    Waardenburg Shah syndrome Associated morphology False Congenital hypopigmentation Inferred relationship Existential restriction modifier 3

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