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721837000: Hypertrichosis and acromegaloid facial appearance syndrome (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    3326201015 Hypertrichosis acromegaloid facial features syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3326202010 Hypertrichosis coarse face syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3326205012 Hypertrichosis and acromegaloid facial appearance syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3326206013 Hypertrichosis and acromegaloid facial appearance syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3326203017 A very rare multiple congenital abnormality syndrome manifesting from birth with progressive hypertrichosis congenita terminalis (thick scalp hair extending onto the forehead with generalized increased body hair) associated with a typical acromegaloid facial appearance (thick eyebrows, prominent supraorbital ridges, broad nasal bridge, anteverted nares, long and large philtrum, and prominent mouth with full lips) appearing during childhood. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3326204011 A very rare multiple congenital abnormality syndrome manifesting from birth with progressive hypertrichosis congenita terminalis (thick scalp hair extending onto the forehead with generalised increased body hair) associated with a typical acromegaloid facial appearance (thick eyebrows, prominent supraorbital ridges, broad nasal bridge, anteverted nares, long and large philtrum, and prominent mouth with full lips) appearing during childhood. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3326201015 Hypertrichosis acromegaloid facial features syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3326201015 Hypertrichosis acromegaloid facial features syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3326202010 Hypertrichosis coarse face syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3326202010 Hypertrichosis coarse face syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3326205012 Hypertrichosis and acromegaloid facial appearance syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3326205012 Hypertrichosis and acromegaloid facial appearance syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3326206013 Hypertrichosis and acromegaloid facial appearance syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3326206013 Hypertrichosis and acromegaloid facial appearance syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3326203017 A very rare multiple congenital abnormality syndrome manifesting from birth with progressive hypertrichosis congenita terminalis (thick scalp hair extending onto the forehead with generalized increased body hair) associated with a typical acromegaloid facial appearance (thick eyebrows, prominent supraorbital ridges, broad nasal bridge, anteverted nares, long and large philtrum, and prominent mouth with full lips) appearing during childhood. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3326204011 A very rare multiple congenital abnormality syndrome manifesting from birth with progressive hypertrichosis congenita terminalis (thick scalp hair extending onto the forehead with generalised increased body hair) associated with a typical acromegaloid facial appearance (thick eyebrows, prominent supraorbital ridges, broad nasal bridge, anteverted nares, long and large philtrum, and prominent mouth with full lips) appearing during childhood. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3431491001000110 Syndrom des akromegaloiden Gesichtes mit Hypertrichose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    950871000172110 HAFF - hypertrichosis, acromegaloid facial features fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    1020121000172111 syndrome d'hypertrichose-faciès acromégaloïde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    950871000172110 HAFF - hypertrichosis, acromegaloid facial features fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    1020121000172111 syndrome d'hypertrichose-faciès acromégaloïde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    3431491001000110 Syndrom des akromegaloiden Gesichtes mit Hypertrichose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Is a Congenital hypertrichosis (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Is a Multiple malformation syndrome with facial defects as major feature false Inferred relationship Existential restriction modifier (core metadata concept)
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Is a Hereditary disorder of the integument (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Finding site Hair structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Finding site Face structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Finding site Hair structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Finding site Face structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Associated morphology Growth alteration false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Associated morphology Growth alteration false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Syndrom des akromegaloiden Gesichtes mit Hypertrichose Is a Developmental hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

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

    REPLACED BY association reference set (foundation metadata concept)

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