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253828000: Mullerian aplasia (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
377915012 Mullerian aplasia en Synonym Active Entire term case sensitive SNOMED CT core module
644635015 Mullerian aplasia (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3786955011 Müllerian duct failure en Synonym Active Entire term case sensitive SNOMED CT core module
3792846014 Aplasia of Müllerian ducts en Synonym Active Only initial character case insensitive SNOMED CT core module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mullerian aplasia Is a Congenital absence of uterus false Inferred relationship Existential restriction modifier
Mullerian aplasia Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Mullerian aplasia Finding site Entire genital organ false Inferred relationship Existential restriction modifier 2
Mullerian aplasia Course Multiple superficial injuries of lower leg false Inferred relationship Existential restriction modifier
Mullerian aplasia Occurrence Congenital false Inferred relationship Existential restriction modifier
Mullerian aplasia Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Mullerian aplasia Finding site Uterine structure false Inferred relationship Existential restriction modifier 1
Mullerian aplasia Finding site Female genital tract false Inferred relationship Existential restriction modifier
Mullerian aplasia Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Mullerian aplasia Finding site Uterine structure false Inferred relationship Existential restriction modifier 1
Mullerian aplasia Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Mullerian aplasia Finding site Uterine structure false Inferred relationship Existential restriction modifier 2
Mullerian aplasia Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 2
Mullerian aplasia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Mullerian aplasia Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Mullerian aplasia Finding site Entire uterus false Inferred relationship Existential restriction modifier 1
Mullerian aplasia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Mullerian aplasia Associated morphology Agenesis false Inferred relationship Existential restriction modifier 1
Mullerian aplasia Is a Disorder of embryonic structure true Inferred relationship Existential restriction modifier
Mullerian aplasia Is a Congenital malformation true Inferred relationship Existential restriction modifier
Mullerian aplasia Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Mullerian aplasia Associated morphology Aplasia true Inferred relationship Existential restriction modifier 1
Mullerian aplasia Finding site Structure of paramesonephric duct true Inferred relationship Existential restriction modifier 1
Mullerian aplasia Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
WNT4 Müllerian aplasia and ovarian dysfunction Is a True Mullerian aplasia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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