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900000000000509007: United States of America English language reference set (foundation metadata concept)


Status: current, estado de definición de concepto necesario pero no suficiente (metadato del núcleo). Date: 31-Jan 2002. Module: módulo identificador para componentes del modelo de SNOMED CT (metadato del núcleo)

Descriptions:

Id Description Lang Type Status Case? Module
2911457018 conjunto de referencias de idioma inglés de acuerdo con la ortografía de Estados Unidos de Norteamérica es sinónimo (metadato del núcleo) Active letras mayúsculas y minúsculas relevantes en todo el término (metadato del núcleo) Latin American Spanish extension module
2911675011 conjunto de referencias de idioma inglés de acuerdo con la ortografía de Estados Unidos de Norteamérica (metadato fundacional) es descripción completa Active letras mayúsculas y minúsculas relevantes en todo el término (metadato del núcleo) Latin American Spanish extension module
2911702016 inglés estadounidense es sinónimo (metadato del núcleo) Active uso de mayúsculas y minúsculas sin relevancia para la totalidad del término (metadato del núcleo) Latin American Spanish extension module
900000000001115012 United States of America English language reference set en sinónimo (metadato del núcleo) Active letras mayúsculas y minúsculas relevantes en todo el término (metadato del núcleo) módulo identificador para componentes del modelo de SNOMED CT (metadato del núcleo)
900000000001116013 US English en sinónimo (metadato del núcleo) Active letras mayúsculas y minúsculas relevantes en todo el término (metadato del núcleo) módulo identificador para componentes del modelo de SNOMED CT (metadato del núcleo)
900000000001117016 United States of America English language reference set (foundation metadata concept) en descripción completa Active letras mayúsculas y minúsculas relevantes en todo el término (metadato del núcleo) módulo identificador para componentes del modelo de SNOMED CT (metadato del núcleo)


1321854 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
conjunto de referencias de idioma inglés de acuerdo con la ortografía de Estados Unidos de Norteamérica (metadato fundacional) es un[a] conjunto de referencias de lenguaje para el idioma inglés true relación inferida restricción existencial (metadato del núcleo)

Members acceptabilityId
46,XY disorder of sex development, adrenal insufficiency due to cytochrome P450 family 11 subfamily A member 1 deficiency (disorder) preferido
46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome preferido
46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome (disorder) preferido
46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome is a rare, genetic, developmental defect during embryogenesis disorder characterized by partial (unilateral testis, persistence of Müllerian duct structures) or complete (streak gonads only) gonadal dysgenesis, usually manifesting with primary amenorrhea in individuals with female phenotype but 46,XY karyotype, and sensorimotor dysmyelinating minifascicular polyneuropathy, which presents with numbness, weakness, exercise-induced muscle cramps, sensory disturbances and reduced/absent deep tendon reflexes. Germ cell tumors (seminoma, dysgerminoma, gonadoblastoma) may develop from the gonadal tissue. preferido
46,XY ovotesticular disorder of sex development preferido
46,XY ovotesticular disorder of sex development (disorder) preferido
46,XY ovotesticular disorder of sex development is a rare, genetic disorder of sex development characterized by either the coexistence of both male and female reproductive gonads or, more frequently, by the presence of one or both gonads containing a mixture of both testicular and ovarian tissue (ovotestes) in an individual with a normal male 46, XY karyotype. External genitalia are usually ambiguous but can range from normal male to normal female and if a uterus and/or fallopian tubes are present, they are generally hypoplastic. Cryptorchidism, hypospadias, infertility and increased risk of gonadal tumors are frequently associated. preferido
46,XY partial gonadal dysgenesis preferido
46,XY partial gonadal dysgenesis (disorder) preferido
460 preferido
460 (qualifier value) preferido
467 preferido
467 (qualifier value) preferido
469.01 preferido
469.01 (qualifier value) preferido
46XX preferido
46XX (qualifier value) preferido
47 (AJCC) aceptable (metadato fundacional)
47 (UICC) aceptable (metadato fundacional)
47,XYY syndrome aceptable (metadato fundacional)
47-Ca aceptable (metadato fundacional)
475 preferido
475 (qualifier value) preferido
48 preferido
48 (AJCC) aceptable (metadato fundacional)
48 (UICC) aceptable (metadato fundacional)
48 (qualifier value) preferido
48 hour ambulatory electrocardiographic monitoring preferido
48 hour ambulatory electrocardiographic monitoring (procedure) preferido
48 hour fecal specimen aceptable (metadato fundacional)
48 hour stool specimen preferido
48 hour urine specimen preferido
48 hours preferido
48 hours (qualifier value) preferido
48,XXXX syndrome aceptable (metadato fundacional)
48,XYYY syndrome preferido
48,XYYY syndrome (disorder) preferido
48-Cr aceptable (metadato fundacional)
48-V aceptable (metadato fundacional)
48.19 preferido
48.19 (qualifier value) preferido
48.2 preferido
48.2 (qualifier value) preferido
480 preferido
480 (qualifier value) preferido
48000 preferido
48000 (qualifier value) preferido
48000000 preferido
48000000 (qualifier value) preferido
49 (AJCC) aceptable (metadato fundacional)
49 (UICC) aceptable (metadato fundacional)
49,XXXYY syndrome preferido
49,XXXYY syndrome (disorder) preferido
49,XXXYY syndrome is a rare gonosome anomaly syndrome characterized by a eunuchoid habitus with gynecoid fat distribution and shape, normal to tall stature, moderate to severe intellectual disability, distinctive facial features (e.g. prominent forehead, epicanthic folds, broad nasal bridge, prognathism), gynecomastia, hypogonadism, cryptorchidism, small penis and behavioral abnormalities (including solitary, passive disposition but prone to aggressive outbursts, autistic). Skeletal malformations, such as delayed bone age, fifth finger clinodactyly, elbow malformations and slow molar development, may also be associated. preferido
49,XYYYY syndrome preferido
49,XYYYY syndrome (disorder) preferido
49-V aceptable (metadato fundacional)
493 Poland preferido
4A (AJCC) aceptable (metadato fundacional)
4A (UICC) aceptable (metadato fundacional)
4A1 (AJCC) aceptable (metadato fundacional)
4A1 (UICC) aceptable (metadato fundacional)
4A2 (AJCC) aceptable (metadato fundacional)
4A2 (UICC) aceptable (metadato fundacional)
4B (AJCC) aceptable (metadato fundacional)
4B (UICC) aceptable (metadato fundacional)
4C (AJCC) aceptable (metadato fundacional)
4C (UICC) aceptable (metadato fundacional)
4D (four dimensional) ultrasonography aceptable (metadato fundacional)
4D (four dimensional) ultrasound aceptable (metadato fundacional)
4D (four dimensional) ultrasound scan aceptable (metadato fundacional)
4Fr aceptable (metadato fundacional)
4H leukodystrophy preferido
4H leukodystrophy (disorder) preferido
4H post incubation aceptable (metadato fundacional)
4H post peritoneal dialysis aceptable (metadato fundacional)
4H specimen aceptable (metadato fundacional)
4H specimen aceptable (metadato fundacional)
4H syndrome aceptable (metadato fundacional)
4KB5 aceptable (metadato fundacional)
4a preferido
4a-hydroxytetrahydrobiopterin dehydratase preferido
4a-hydroxytetrahydrobiopterin dehydratase (substance) preferido
4ab preferido
4b preferido
4c preferido
4d preferido
4e preferido
4f preferido
4p minus syndrome aceptable (metadato fundacional)
4p partial monosomy syndrome preferido
4p partial monosomy syndrome (disorder) preferido
4p partial trisomy syndrome preferido
4p partial trisomy syndrome (disorder) preferido
4p16.3 microduplication syndrome preferido
4p16.3 microduplication syndrome (disorder) preferido
4p16.3 microduplication syndrome is a rare genetic syndrome that results from the partial duplication of the short arm of chromosome 4. It has a highly variable phenotype, principally characterized by psychomotor and language delay, seizures and dysmorphic features such as high forehead with frontal bossing, hypertelorism, prominent glabella, long narrow palpebral fissures, low set ears and short neck. Eye abnormalities (glaucoma, irregular iris pigmentation, hyperopia) have also been reported. preferido
4q partial monosomy syndrome preferido
4q partial monosomy syndrome (disorder) preferido
4q partial trisomy syndrome preferido
4q partial trisomy syndrome (disorder) preferido

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Reference Sets

Latin American Spanish language reference set

Chile language reference set (foundation metadata concept)

conjunto de referencias descriptivas de la estructura de otros conjuntos de referencias

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