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900000000000531004: REFERS TO concept 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
900000000001166019 REFERS TO concept association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)
900000000001167011 REFERS TO concept 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)

3685 members. Search Members:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
REFERS TO concept association reference set Is a Historical association reference set (foundation metadata concept) true Inferred relationship Some
Members targetComponentId
Bilirubin, conjugated measurement, serum Serum conjugated bilirubin measurement
Bilirubin-delta Bilirubin-albumin complex
Bilobate placenta Bilobate placenta
Biological aortic valve replacement Replacement of aortic valve with tissue graft
Bioprosthetic aortic valve replacement Replacement of aortic valve with tissue graft
Biopterin Biopterin
Bipartite placenta Bilobate placenta
Bipolar I disorder, most recent episode depressed Bipolar I disorder, most recent episode depression (disorder)
Bipolar I disorder, most recent episode manic Bipolar I disorder, most recent episode manic
Bipolar affective disorder, current episode hypomanic Bipolar I disorder, current episode hypomanic
Birt-Hogg-Dube syndrome A rare inherited cancer-predisposing syndrome characterized by skin lesions, kidney tumors, and pulmonary cysts that may be associated with pneumothorax. The kidney tumors range from benign oncocytomas to malignant renal cell carcinomas including chromophobe, clear cell or papillary subtypes. Fibrofolliculomas are characterized by a circumscribed proliferation of collagen and fibroblasts surrounding distorted hair follicles from which basaloid cells protrude into the surrounding fibromucinous stroma. Other characteristic skin anomalies are trichodiscomas and acrochordons. Dermatological manifestations usually develop in the third and fourth decades of life and persist indefinitely. The syndrome is transmitted in an autosomal dominant fashion.
Birt-Hogg-Dubé syndrome A rare inherited cancer-predisposing syndrome characterized by skin lesions, kidney tumors, and pulmonary cysts that may be associated with pneumothorax. The kidney tumors range from benign oncocytomas to malignant renal cell carcinomas including chromophobe, clear cell or papillary subtypes. Fibrofolliculomas are characterized by a circumscribed proliferation of collagen and fibroblasts surrounding distorted hair follicles from which basaloid cells protrude into the surrounding fibromucinous stroma. Other characteristic skin anomalies are trichodiscomas and acrochordons. Dermatological manifestations usually develop in the third and fourth decades of life and persist indefinitely. The syndrome is transmitted in an autosomal dominant fashion.
Birth asphyxia with 1 minute Apgar score 0-3 Severe birth asphyxia, Apgar 0-3
Birth asphyxia with 1 minute Apgar score 4-7 Mild to moderate birth asphyxia - Apgar score 4-7 at 1 minute
Bite of nonvenomous snake or lizard Lizard bite (event)
Bite of nonvenomous snake or lizard Snake bite
Black eye Periorbital hematoma
Bladder evacuation Evacuation of urinary bladder contents
Bladder instability Overactive urinary bladder (disorder)
Bladder neck stenosis Stenosis of neck of urinary bladder (disorder)
Blastocyst Blastocyst structure
Blastomere Structure of blastomere
Blau syndrome Blau syndrome (BS) is a rare systemic inflammatory disease characterized by early onset granulomatous arthritis, uveitis and skin rash. BS now refers to both the familial and sporadic (formerly early-onset sarcoidosis) form of the same disease. The proposed term pediatric granulomatous arthritis is currently questioned since it fails to represent the systemic nature of the disease.
Bleb A fluid-filled, raised, often translucent lesion, greater than 1 cm in diameter
Blisters in ear canal Blister of external auditory canal
Bloat Abdominal bloating (finding)
Bloat Bloated face
Bloated abdomen Abdominal bloating (finding)
Bloating Abdominal bloating (finding)
Bloating Bloated face
Blood draw Phlebotomy (procedure)
Blood vessel thrombosis Thrombosis of blood vessel (disorder)
Blue green algae poisoning Blue-green algae toxin poisoning
Body height The distance from the base to the top of a subject's entire body.
Body of sphenoid bone Structure of body of sphenoid bone (body structure)
Bombyx mori protein Silkworm protein
Bond orthodontic bracket Fixation of orthodontic bracket to enamel of tooth using bonding agent (procedure)
Bone clip Bone clamp (physical object)
Bone division and displacement Division and displacement of bone (procedure)
Bone flap Bone flap
Bone marrow Bone marrow structure
Bone marrow bony trabeculae Structure of bone marrow bony trabeculae
Bone marrow failure Bone marrow disorder
Bone marrow fatty tissue Structure of bone marrow fatty tissue
Bone marrow of sternum Sternal bone marrow structure (body structure)
Bone marrow of vertebral body Structure of bone marrow of vertebral body
Bone of wrist Bone structure of wrist region
Bone structure of left hip Structure of left innominate bone
Bone structure of right hip Structure of right innominate bone (body structure)
Boston exanthem Exanthem caused by human echovirus 16 (disorder)
Botryoid sarcoma Botryoid sarcoma (morphologic abnormality)
Bovine plasmin Bovine fibrinolysin
Brachytherapy Brachytherapy (procedure)
Brachytherapy procedure Brachytherapy (procedure)
Brailsford's disease A rare bone disease characterized by spontaneous adult-onset tarsal navicular osteonecrosis. Patients present with chronic mid- and hindfoot pain, swelling and tenderness over the dorsomedial aspect of the midfoot, flattening of the medial longitudinal arch, and pes planovarus. Radiographic findings include comma-shaped deformity due to collapse of the lateral part of the navicular bone and medial or dorsal protrusion of a portion or the entire bone. The condition may be bilateral or asymmetric and associated with pathological fractures.
Brain tumor Neoplasm of brain
Brain tumour Neoplasm of brain
Branch of brachial plexus Nerve of brachial plexus distribution
Branch of cervical plexus Nerve of cervical plexus distribution
Branch of sacral plexus Nerve of sacral plexus distribution
Branchial cleft Persistent branchial cleft (morphologic abnormality)
Breast abscess after childbirth Postpartum abscess of breast (disorder)
Breast discharge Discharge from breast (finding)
Breathing in Inspiration
Brenner tumor Benign Brenner tumour
Brenner tumor Brenner tumor, malignant
Brenner tumor Brenner tumor, borderline malignancy
Brenner tumour Brenner tumor, malignant
Brenner tumour Brenner tumor, borderline malignancy
Brenner tumour Benign Brenner tumour
Bridge or pontic hygiene care instruction Bridge or pontic hygiene care education (procedure)
Briquet's disorder Briquet's syndrome (disorder)
Broadbills Genus Myiagra (organism)
Broadbills Genus Myiagra (organism)
Broken teeth Fracture of teeth (disorder)
Bromelain Bromelains (substance)
Bronchial adenoma, cylindroid Bronchial adenomatous neoplasm
Bronchial brushing cytologic material Bronchial brushings specimen
Bronchial washing Lavage of bronchus
Bronchial washing cytologic material Specimen from lung obtained by bronchial washing procedure
Bubble stability test Bubble stability test technique
Bubble stability test Bubble stability test in amniotic fluid
Burn leg/foot - erythema Epidermal burn of foot (disorder)
Burn leg/foot - erythema Epidermal burn of lower leg
Burning oral sensation Burning sensation of mouth
Burning vulva Burning sensation of vulva
Bursa of olecranon Structure of bursa of olecranon (body structure)
Byler syndrome An infantile hereditary disorder of bile formation that is hepatocellular in origin and associated with extrahepatic features. Onset occurs mostly during infancy with clinical signs of cholestasis with recurrent or permanent jaundice associated with hepatomegaly and severe pruritus. Caused by mutations in the ATP8B1 gene (18q21-22) encoding the FIC1 protein expressed at the canalicular membrane of hepatocytes as well as in other epithelia. Transmission is autosomal recessive.
C cell carcinoma Medullary thyroid carcinoma (morphologic abnormality)
C cell neuroendocrine neoplasm Medullary thyroid carcinoma (morphologic abnormality)
CA - Cancer of spine Malignant neoplasm of vertebral column region (disorder)
CAT scan of head CT of head
CAVG - Coronary artery vein graft Aortocoronary artery bypass graft with vein graft
CFA - Balloon angioplasty of common femoral artery Percutaneous transluminal balloon angioplasty of common femoral artery using fluoroscopic guidance with contrast (procedure)
CHT - Congenital hypothyroidism Congenital hypothyroidism
CIA - Balloon angioplasty of the common iliac artery Percutaneous transluminal balloon angioplasty of common iliac artery using fluoroscopic guidance with contrast (procedure)
CIT - Cautery to inferior turbinate Cauterization of inferior nasal turbinate (procedure)
CLO test for helicobacter pylori CLO test for helicobacter pylori
CT of head CT of head
CT of pelvis and lower extremity with contrast CT of pelvis and lower limb with contrast
CT scan of head CT of head

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