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900000000000526001: REPLACED BY association reference set (foundation metadata concept)


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

Descriptions:

Id Description Lang Type Status Case? Module
900000000001156010 REPLACED BY association reference set (foundation metadata concept) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)
900000000001157018 REPLACED BY association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)


10679 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
REPLACED BY association reference set (foundation metadata concept) Is a Historical association reference set (foundation metadata concept) true Inferred relationship Some

Members targetComponentId
[D]Transaminase or lactic acid dehydrogenase raised Elevated level of transaminase and lactic acid dehydrogenase (finding)
[D]Transient paralysis of a limb Transient limb paralysis
[D]Tremor Tremor
[D]Tympany, chest Chest tympanitic to percussion
[D]Ultrasound cardiogram abnormal Echocardiogram abnormal
[D]Umbilical bleeding Umbilical bleeding (finding)
[D]Umbilical discharge Umbilical discharge
[D]Umbilical mass Umbilical mass
[D]Umbilical pain Umbilical pain
[D]Umbilical swelling Umbilical swelling
[D]Unattended death Unattended death
[D]Unconsciousness Unconscious (finding)
[D]Underweight Underweight
[D]Undue concern and preoccupation with stressful events Undue concern and preoccupation with stressful events
[D]Unhappiness Feeling unhappy (finding)
[D]Ureter filling defect Ureter filling defect (finding)
[D]Ureteric colic Ureteric colic
[D]Urethral discharge Urethral discharge
[D]Urethral sphincter incontinence Urinary incontinence due to urethral sphincter incompetence (finding)
[D]Urethrorrhea Urethral discharge
[D]Urgency of micturition Urgent desire to urinate
[D]Vaginal fluid abnormal Vaginal fluid abnormal
[D]Vectorcardiogram abnormal Vectorcardiogram abnormal
[D]Verbosity and circumstantial detail obscuring reason for contact Verbosity and circumstantial detail obscuring reason for contact
[D]Very low level of personal hygiene Very low level of personal hygiene (finding)
[D]Vesical pain Bladder pain
[D]Vesical tenesmus Painful bladder spasm
[D]Visible peristalsis Visible peristalsis
[D]Visual hallucinations Visual hallucinations
[D]Visually evoked potentials abnormal Abnormal visual evoked potential
[D]Vital capacity reduced Vital capacity reduced
[D]Vomiting Vomiting (disorder)
[D]Wasting disease Wasting disease
[D]Waterbrash Waterbrash
[D]Weak pulse Thready pulse
[D]Weight, failure to gain, infant Failure to thrive in infant (disorder)
[D]Wheezing Wheezing
[D]Wrist lump Mass of wrist
[D]Yawning Yawning
[D]Zinc, blood level abnormal Abnormal zinc level in blood
[M]Acute myeloid leukaemia Acute myeloid leukemia (morphologic abnormality)
[M]Aleukaemic monocytic leukaemia Aleukaemic monocytic leukaemia
[M]Angiofibroma NOS Angiofibroma (morphologic abnormality)
[M]Chronic leukaemia NOS Chronic leukemia
[M]Chronic monocytic leukaemia Chronic monocytic leukemia
[M]Chronic monocytic leukaemia Chronic myeloid leukemia (morphologic abnormality)
[M]Haemangiopericytic neoplasms Solitary fibrous tumor
[M]Malignant melanoma NOS or melanocarcinoma or melanoma NOS Malignant melanoma
[M]Monocytic leukaemia NOS Monocytic leukaemia
[M]Other lymphoid leukaemia NOS Lymphoid leukaemia
[M]Plasmacytoma NOS Plasmacytoma (disorder)
[M]Subacute monocytic leukaemia Subacute monocytic leukaemia
[M]Subacute monocytic leukaemia Subacute monocytic leukaemia
[X] (Unspecified organic personality and behavioural disorder due to brain disease, damage and dysfunction) or (organic psychosyndrome) Organic mental disorder
alpha-Aminoacylpeptide hydrolase Alpha-aminoacylpeptide hydrolase (substance)
beta Carotene Betacarotene
cDE genotype cDE haplotype (finding)
cDe genotype cDe haplotype (finding)
cdE genotype cdE haplotype (finding)
cde genotype cde haplotype (finding)
de Quervain's disease Radial styloid tenosynovitis
kV kilovolt
lotrozole Product containing letrozole (medicinal product)
mA mA - milliampere
mV millivolt (qualifier value)
n-1-Naphthyl sodium salt Herbicide
p-Amino diphenylamine 4-aminobiphenyl (substance)
pN0(i+): No regional lymph node metastasis histologically, positive IHC, no IHC cluster greater than 0.2 mm (breast) pN0(i+): No regional lymph node metastasis histologically, positive morphologic findings for isolated tumor cells, no cluster greater than 0.2 mm (breast) (finding)
pN0(i-): No regional lymph node metastasis histologically, negative IHC (breast) pN0(i-): No regional lymph node metastasis histologically, negative morphologic findings for isolated tumor cells (breast) (finding)
pN0(mol+): No regional lymph node metastasis histologically, positive molecular findings (breast) pN0(mol+): No regional lymph node metastasis histologically, positive nonmorphologic (molecular) findings for isolated tumor cells (breast) (finding)
pN0(mol-): No regional lymph node metastasis histologically, negative molecular findings (breast) pN0(mol-): No regional lymph node metastasis histologically, negative nonmorphologic (molecular) findings for isolated tumor cells (breast) (finding)
pT4a: direkt tumörinväxt i andra organ eller strukturer (kolon/rektum) pT4a: Tumor penetrates to surface of visceral peritoneum (colon/rectum) (finding)
pT4b: Tumor involves masticator space, pterygoid plates, or skull base and/or encases internal carotid artery (oropharynx) pT4b: Tumor invades lateral pterygoid muscle, pterygoid plates, lateral nasopharynx, or skull base or encases internal carotid artery (oropharynx) (finding)
pT4b: tumör penetrerar viscerala peritoneum (kolon/rektum) pT4b: Tumor directly invades or is adherent to other organs or structures (colon/rectum) (finding)
para-aminohippuric acid Para-aminohippuric acid
r phenotype cde haplotype (finding)
r'' phenotype cdE haplotype (finding)
ry phenotype CdE haplotype (finding)
von Willebrand disease von Willebrand disorder

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