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58672003: Reifenstein syndrome (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    97496014 Reifenstein syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    97497017 Lubs syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    97498010 Gilbert-Dreyfuss syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    97499019 Rosewater syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    97500011 Familial incomplete male pseudohermaphroditism, type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    797430010 Reifenstein syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    1231866014 Reifenstein's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    97496014 Reifenstein syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    97497017 Lubs syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    97498010 Gilbert-Dreyfuss syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    97499019 Rosewater syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    97499019 Rosewater syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    97500011 Familial incomplete male pseudohermaphroditism, type 1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    97500011 Familial incomplete male pseudohermaphroditism, type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    797430010 Reifenstein syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    797430010 Reifenstein syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    1231866014 Reifenstein's syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1231866014 Reifenstein's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Reifenstein syndrome Is a Congenital anomaly of endocrine gland false Inferred relationship Existential restriction modifier (core metadata concept)
    Reifenstein syndrome Is a Male pseudohermaphroditism false Inferred relationship Existential restriction modifier (core metadata concept)
    Reifenstein syndrome Is a Disorder of androgen receptor (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Reifenstein syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Reifenstein syndrome Finding site Entire genital organ (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Reifenstein syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Reifenstein syndrome Finding site Male structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Reifenstein syndrome Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Reifenstein syndrome Course Multiple superficial injuries of lower leg false Inferred relationship Existential restriction modifier (core metadata concept)
    Reifenstein syndrome Is a A disorder of sex development (DSD) characterised by the presence of female external genitalia, ambiguous genitalia or variable defects in virilisation in a 46,XY individual with absent or partial responsiveness to age-appropriate levels of androgens. It comprises two clinical subgroups: complete AIS (CAIS) and partial AIS (PAIS). false Inferred relationship Existential restriction modifier (core metadata concept)
    Reifenstein syndrome Finding site Genital structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Reifenstein syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Reifenstein syndrome Is a Congenital anomaly of endocrine gonad (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Reifenstein syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Reifenstein syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Reifenstein syndrome Finding site Genital structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Reifenstein syndrome Finding site Gonadal endocrine structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Reifenstein syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Reifenstein syndrome Finding site Genital structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Reifenstein syndrome Finding site Gonadal endocrine structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Reifenstein syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Reifenstein syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Reifenstein syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Reifenstein syndrome Finding site Genital structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Reifenstein syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Reifenstein syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Reifenstein syndrome Finding site Gonadal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Reifenstein syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Reifenstein syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Reifenstein syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Reifenstein syndrome Finding site External genitalia structure false Inferred relationship Existential restriction modifier (core metadata concept) 2

    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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