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71934003: Genital structure (body structure)

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
502003018 Genital structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
812155011 Genital structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1543 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Genital structure Is a This structure, also termed the pelvic region, includes the wall, cavity and content of both the true and false pelvis; it consequently incorporates the entire bony pelvis; and inferiorly it is bounded and includes the pelvic diaphragm. The structure incorporates the complete pelvic wall; sacrococcygeal region (including the overlying skin and subcutaneous tissue); the contents of the false pelvic cavity; but in contrast to the 'pelvic segment of trunk' excludes the perineum, external genitalia. false Inferred relationship Some
Genital structure Is a Structure of anatomical reproductive system (body structure) true Inferred relationship Some
Genital structure partie de Entire genitourinary system false Additional relationship Some
Genital structure partie de Surface region of lower trunk false Additional relationship Some
Genital structure partie de Entire female false Inferred relationship Some
Genital structure Is a Structure of genitourinary system (body structure) false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Pathogen-negative nonspecific genital infection Finding site True Genital structure Inferred relationship Some 1
Fishing hook in genitalia Finding site True Genital structure Inferred relationship Some 1
X-ray female external genitalia Procedure site - Direct (attribute) False Genital structure Inferred relationship Some 2
Normal genitalia Finding site True Genital structure Inferred relationship Some 2
Gender confirmation bottom surgery Procedure site - Direct (attribute) False Genital structure Inferred relationship Some 1
46,XY disorder of sex development Finding site True Genital structure Inferred relationship Some 1
Gender confirmation phalloplasty Procedure site - Direct (attribute) False Genital structure Inferred relationship Some 1
Gender confirmation metoidioplasty Procedure site - Direct (attribute) False Genital structure Inferred relationship Some 1
46,XY disorder of sex development due to environmental chemical exposure (disorder) Finding site True Genital structure Inferred relationship Some 1
46,XX disorder of sex development Finding site True Genital structure Inferred relationship Some 1
Superficial injury of genitalia Finding site True Genital structure Inferred relationship Some 1
Anogenital ulceration due to Behcet disease Finding site True Genital structure Inferred relationship Some 2
Pseudohermaphroditism due to congenital adrenal hyperplasia (disorder) Finding site True Genital structure Inferred relationship Some 1
Macrogenitosomia praecox due to disorder of pineal gland (disorder) Finding site True Genital structure Inferred relationship Some 2
A rare difference of sex development due to reduced 17,20-lyase activity that affects individuals with 46,XY karyotype and is characterized by female or atypical external genitalia with reduced phallic size, hypospadias, incomplete fusion of the labioscrotal swellings, cryptorchidism, and a blind vaginal pouch. Blood pressure and electrolytes are normal whilst hormonal investigations show normal basal and stimulated levels of cortisol, and low basal and stimulated androgen levels. Finding site True Genital structure Inferred relationship Some 1
A rare genetic disease characterized by pre- and postnatal growth restriction, developmental delay, adrenal hypoplasia, genital abnormalities (such as microphallus, hypospadias, or cryptorchidism), thrombocytopenia and/or anemia, recurrent severe invasive infections, and enteropathy with chronic diarrhea. Myelodysplastic syndrome and dysmorphic features (including downslanting palpebral fissures, low-set and posteriorly rotated ears, anteverted nares, camptodactyly, and arachnodactyly, among others) may also be observed. Finding site True Genital structure Inferred relationship Some 1
Therapeutic aspiration of hydrocele Procedure site - Indirect (attribute) True Genital structure Inferred relationship Some 1
A rare autoinflammatory syndrome with characteristics of the presence of features of relapsing polychondritis and Behcet disease in the same individual. This includes cartilage inflammation of the ears, nose, throat and rib cage as well as recurrent oral and genital ulcers respectively. Patients may also present ocular involvement (in particular anterior uveitis or scleritis), arthritis, fever, colitis, thrombophlebitis, and central nervous system vasculitis or in rare cases arterial aneurysms. Symptoms of polychondritis occur secondary to those of Behcet disease in the vast majority of cases. Finding site True Genital structure Inferred relationship Some 5
Pruritus of genital organs Finding site True Genital structure Inferred relationship Some 2
Latent genital herpes simplex during pregnancy (disorder) Finding site True Genital structure Inferred relationship Some 1
Chylorrhea of external genitalia (disorder) Finding site True Genital structure Inferred relationship Some 1
Plain X-ray of genital (procedure) Procedure site - Direct (attribute) True Genital structure Inferred relationship Some 1
Swab from genital ulcer (specimen) Specimen source topography True Genital structure Inferred relationship Some 1
Combined urethral and genital swab Specimen source topography True Genital structure Inferred relationship Some 2

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

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