26896004: Structure of paramesonephric duct (body structure)

SNOMED CT Concept\Body structure (body structure)\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\Developmental body structure\Embryonic structure\Embryo structure\Structure of embryonic urogenital system (body structure)\Embryonic urinary tract structure\Nephrogenic cord derivative\Mesonephric structure\Structure of paramesonephric duct

\Body region structure\Structure of half of body lateral to midsagittal plane (body structure)\Nephrogenic cord derivative\Mesonephric structure\Structure of paramesonephric duct

\Structure of product of conception\Embryonic structure\Embryo structure\Structure of embryonic urogenital system (body structure)\Embryonic urinary tract structure\Nephrogenic cord derivative\Mesonephric structure\Structure of paramesonephric duct

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

45001018 Paramesonephric duct en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

45002013 Mullerian duct en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

483373010 Structure of paramesonephric duct en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

757400013 Structure of paramesonephric duct (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Structure of paramesonephric duct	Is a	Mesonephric structure	true	Inferred relationship	Some
Structure of paramesonephric duct	partie de	Entire embryo	false	Additional relationship	Some
Structure of paramesonephric duct	Laterality	Side (qualifier value)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Entire paramesonephric duct	Is a	True	Structure of paramesonephric duct	Inferred relationship	Some
Excision of cyst of Müllerian duct in male	Procedure site	False	Structure of paramesonephric duct	Inferred relationship	Some
Excision of Müllerian duct	Procedure site	False	Structure of paramesonephric duct	Inferred relationship	Some	1
Excision of cyst of Müllerian duct in male	Procedure site - Indirect (attribute)	False	Structure of paramesonephric duct	Inferred relationship	Some	1
Excision of Müllerian duct	Procedure site - Direct (attribute)	False	Structure of paramesonephric duct	Inferred relationship	Some	1
Excision of cyst of Müllerian duct in male	Procedure site - Direct (attribute)	False	Structure of paramesonephric duct	Inferred relationship	Some	1
Excision of cyst of Müllerian duct in male	Procedure site - Direct (attribute)	True	Structure of paramesonephric duct	Inferred relationship	Some	1
Excision of Müllerian duct	Procedure site - Direct (attribute)	True	Structure of paramesonephric duct	Inferred relationship	Some	1
Mullerian remnant	Finding site	False	Structure of paramesonephric duct	Inferred relationship	Some	2
Persistent Müllerian duct syndrome	Finding site	True	Structure of paramesonephric duct	Inferred relationship	Some	1
Mullerian remnant	Finding site	True	Structure of paramesonephric duct	Inferred relationship	Some	1
A rare disorder characterized by the association of mullerian duct and distal limb anomalies. Females present with anomalies ranging from a vaginal septum to complete duplication of uterus and vagina, and males present with micropenis. The limb anomalies varied from postaxial polydactyly to severe upper limb hypoplasia with split hand.	Finding site	False	Structure of paramesonephric duct	Inferred relationship	Some	2
Cyst of paramesonephric duct (disorder)	Finding site	True	Structure of paramesonephric duct	Inferred relationship	Some	1
A rare genetic disease characterized by the presence of Müllerian duct derivatives (rudimentary uterus, fallopian tubes, and atretic vagina) and other genital anomalies (cryptorchidism, micropenis) in male newborns, intestinal and pulmonary lymphangiectasia, protein-losing enteropathy, hepatomegaly, and renal anomalies. Postaxial polydactyly, facial dysmorphism (including broad nasal bridge, bulbous nasal tip, long and prominent upper lip with smooth philtrum, hypertrophic alveolar ridges, and mild retrognathia, among other features), and short limbs have also been described. The syndrome is fatal in infancy.	Finding site	False	Structure of paramesonephric duct	Inferred relationship	Some	7
A rare genetic disease characterized by the presence of Müllerian duct derivatives (rudimentary uterus, fallopian tubes, and atretic vagina) and other genital anomalies (cryptorchidism, micropenis) in male newborns, intestinal and pulmonary lymphangiectasia, protein-losing enteropathy, hepatomegaly, and renal anomalies. Postaxial polydactyly, facial dysmorphism (including broad nasal bridge, bulbous nasal tip, long and prominent upper lip with smooth philtrum, hypertrophic alveolar ridges, and mild retrognathia, among other features), and short limbs have also been described. The syndrome is fatal in infancy.	Finding site	True	Structure of paramesonephric duct	Inferred relationship	Some	4
A rare disorder characterized by the association of mullerian duct and distal limb anomalies. Females present with anomalies ranging from a vaginal septum to complete duplication of uterus and vagina, and males present with micropenis. The limb anomalies varied from postaxial polydactyly to severe upper limb hypoplasia with split hand.	Finding site	True	Structure of paramesonephric duct	Inferred relationship	Some	1
Mullerian aplasia	Finding site	True	Structure of paramesonephric duct	Inferred relationship	Some	1
WNT4 Mullerian aplasia and ovarian dysfunction	Finding site	True	Structure of paramesonephric duct	Inferred relationship	Some	2

Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

Anatomy structure and entire association reference set (foundation metadata concept)