FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

58672003: Reifenstein syndrome (disorder)

    Status: retired, Primitive. Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Reifenstein syndrome Occurrence Congenital false Inferred relationship Some 2
    Reifenstein syndrome Pathological process Pathological developmental process false Inferred relationship Some 1
    Reifenstein syndrome Finding site Gonadal structure false Inferred relationship Some 2
    Reifenstein syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Some 1
    Reifenstein syndrome Pathological process Pathological developmental process false Inferred relationship Some 2
    Reifenstein syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Some 2
    Reifenstein syndrome Finding site External genitalia structure false Inferred relationship Some 2
    Reifenstein syndrome Is a Androgen resistance syndrome false Inferred relationship Some
    Reifenstein syndrome Finding site Genital structure false Inferred relationship Some 4
    Reifenstein syndrome Associated morphology Congenital anomaly false Inferred relationship Some 1
    Reifenstein syndrome Is a Congenital anomaly of endocrine gonad false Inferred relationship Some
    Reifenstein syndrome Is a Congenital anomaly of endocrine gland false Inferred relationship Some
    Reifenstein syndrome Is a Male pseudohermaphroditism false Inferred relationship Some
    Reifenstein syndrome Is a Disorder of androgen receptor false Inferred relationship Some
    Reifenstein syndrome Occurrence Congenital false Inferred relationship Some
    Reifenstein syndrome Associated morphology Congenital malformation false Inferred relationship Some 2
    Reifenstein syndrome Finding site Genital structure false Inferred relationship Some 2
    Reifenstein syndrome Finding site Gonadal endocrine structure false Inferred relationship Some 1
    Reifenstein syndrome Associated morphology Congenital malformation false Inferred relationship Some 2
    Reifenstein syndrome Finding site Genital structure false Inferred relationship Some 2
    Reifenstein syndrome Finding site Gonadal endocrine structure false Inferred relationship Some 1
    Reifenstein syndrome Associated morphology Congenital anomaly false Inferred relationship Some 1
    Reifenstein syndrome Occurrence Congenital false Inferred relationship Some 3
    Reifenstein syndrome Associated morphology Developmental abnormality false Inferred relationship Some 3
    Reifenstein syndrome Finding site Genital structure false Inferred relationship Some 3
    Reifenstein syndrome Associated morphology Developmental abnormality false Inferred relationship Some 2
    Reifenstein syndrome Finding site Entire genital organ false Inferred relationship Some 1
    Reifenstein syndrome Occurrence Congenital false Inferred relationship Some
    Reifenstein syndrome Finding site Male structure false Inferred relationship Some
    Reifenstein syndrome Finding site Entire endocrine gonad false Inferred relationship Some 1
    Reifenstein syndrome Course Multiple superficial injuries of lower leg false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Australian dialect reference set

    Concept inactivation indicator reference set

    Description inactivation indicator reference set

    REPLACED BY association reference set

    Back to Start