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20982000: Structure of capillary blood vessel (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
35276019 Capillary en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5048315017 Structure of capillary blood vessel en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5048316016 Structure of capillary blood vessel (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1038561000241115 capillaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1079421000241118 vaisseau sanguin capillaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1079431000241116 structure d'un capillaire sanguin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1079441000241114 structure du capillaire sanguin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


25 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Structure of capillary blood vessel Is a Blood vessel structure (body structure) true Inferred relationship Some
Structure of capillary blood vessel partie de Entire cardiovascular system false Additional relationship Some
Structure of capillary blood vessel Is a A vessel that could be a lymphatic vessel, arteriole, capillary or venule. true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Capillaritis caused by drug (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Nevus anemicus Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Port-wine stain in proteus syndrome (disorder) Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Capillary malformation Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Thrombotic thrombocytopenic purpura Finding site True Structure of capillary blood vessel Inferred relationship Some 2
Progressive pigmentary dermatosis of Schamberg Finding site False Structure of capillary blood vessel Inferred relationship Some 2
Acquired thrombotic thrombocytopenic purpura (disorder) Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Autoimmune thrombotic thrombocytopenic purpura (disorder) Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Drug induced thrombotic thrombocytopenic purpura (disorder) Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Acquired thrombotic thrombocytopenic purpura (disorder) Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Drug induced thrombotic thrombocytopenic purpura (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Autoimmune thrombotic thrombocytopenic purpura (disorder) Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Eczematid-like purpura of Doucas and Kapetanakis Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Port-wine stain in proteus syndrome (disorder) Finding site False Structure of capillary blood vessel Inferred relationship Some 2
Capillary malformation Finding site False Structure of capillary blood vessel Inferred relationship Some 2
Salmon patch naevus Finding site False Structure of capillary blood vessel Inferred relationship Some 3
Hereditary vascular fragility Finding site False Structure of capillary blood vessel Inferred relationship Some 2
Capillary fragility abnormality Finding site False Structure of capillary blood vessel Inferred relationship Some 4
Nevus anemicus Finding site False Structure of capillary blood vessel Inferred relationship Some 3
Port-wine stain with oculocutaneous melanosis (disorder) Finding site False Structure of capillary blood vessel Inferred relationship Some 2
Port-wine stain with associated anomalies (disorder) Finding site False Structure of capillary blood vessel Inferred relationship Some 2
Port-wine stain in Rubinstein-Taybi syndrome (disorder) Finding site False Structure of capillary blood vessel Inferred relationship Some 2
Port-wine stain associated with spinal dysraphism (disorder) Finding site False Structure of capillary blood vessel Inferred relationship Some 3
Salmon patch naevus Finding site False Structure of capillary blood vessel Inferred relationship Some 2
Nevus anemicus Finding site False Structure of capillary blood vessel Inferred relationship Some 2
Capillary-venous malformation Finding site False Structure of capillary blood vessel Inferred relationship Some 3
Capillary-venous-lymphatic malformation Finding site False Structure of capillary blood vessel Inferred relationship Some 6
Congenital capillary hemangioma (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Phakomatosis cesioflammea Finding site False Structure of capillary blood vessel Inferred relationship Some 5
Phakomatosis spilorosea Finding site False Structure of capillary blood vessel Inferred relationship Some 5
Phakomatosis caesiomarmorata Finding site False Structure of capillary blood vessel Inferred relationship Some 5
Microcephaly-capillary malformation syndrome Finding site False Structure of capillary blood vessel Inferred relationship Some 3
Megalencephaly-capillary malformation syndrome Finding site False Structure of capillary blood vessel Inferred relationship Some 5
Pulmonary capillaritis (disorder) Finding site False Structure of capillary blood vessel Inferred relationship Some 1
A small vessel vasculitis restricted to the lungs that may induce diffuse alveolar hemorrhage without any underlying systemic disease. Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Capillary-venous malformation Finding site True Structure of capillary blood vessel Inferred relationship Some 2
Microcephaly-capillary malformation syndrome Finding site True Structure of capillary blood vessel Inferred relationship Some 2
A rare, complex, vascular malformation syndrome characterized by capillary malformation of the lower lip, lymphatic malformation of the face and neck, asymmetry of face and limbs, and partial or generalized overgrowth involving one or more body segments. Finding site False Structure of capillary blood vessel Inferred relationship Some 5
Platelet embolism (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 1
A life-threatening, rapidly progressive thrombotic disorder affecting mainly neonates and children that is characterized by purpuric skin lesions and disseminated intravascular coagulation. It may progress rapidly to multi-organ failure caused by thrombotic occlusion of small and medium-sized blood vessels. There are two forms of the disorder that are classified according to triggering mechanisms: acute infectious (the most common form), and idiopathic purpura fulminans. Finding site False Structure of capillary blood vessel Inferred relationship Some 5
Senile angioma Finding site True Structure of capillary blood vessel Inferred relationship Some 3
Megalencephaly-capillary malformation syndrome Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Phakomatosis cesioflammea Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Phakomatosis spilorosea Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Phakomatosis caesiomarmorata Finding site True Structure of capillary blood vessel Inferred relationship Some 1
A rare, complex, vascular malformation syndrome characterized by capillary malformation of the lower lip, lymphatic malformation of the face and neck, asymmetry of face and limbs, and partial or generalized overgrowth involving one or more body segments. Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum Finding site False Structure of capillary blood vessel Inferred relationship Some 2
Pulmonary capillary haemangiomatosis Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Capillary hemangioma of eyelid Finding site True Structure of capillary blood vessel Inferred relationship Some 2
Lichen aureus Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Capillary hemangioma of orbit Finding site False Structure of capillary blood vessel Inferred relationship Some 2
Capillary haemangioma of retina Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Capillary hemangioma (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 1
à l'examen : nævi angiomateux multiples Finding site False Structure of capillary blood vessel Inferred relationship Some 3
Capillary haemangioma of right orbit region Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Capillary hemangioma of left orbit region (disorder) Finding site False Structure of capillary blood vessel Inferred relationship Some 1
Megalencephaly capillary malformation Finding site True Structure of capillary blood vessel Inferred relationship Some 2
Structure of capillary of lung Is a True Structure of capillary blood vessel Inferred relationship Some
Acute intravascular thrombotic microangiopathy Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Chronic thrombotic microangiopathy Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Capillary specimen collection Procedure site - Indirect (attribute) True Structure of capillary blood vessel Inferred relationship Some 1
Heel stick (procedure) Procedure site - Indirect (attribute) True Structure of capillary blood vessel Inferred relationship Some 1
Ear lobe stick (procedure) Procedure site - Indirect (attribute) True Structure of capillary blood vessel Inferred relationship Some 1
Thumb-prick sampling Procedure site - Indirect (attribute) True Structure of capillary blood vessel Inferred relationship Some 1
Finger stick Procedure site - Indirect (attribute) True Structure of capillary blood vessel Inferred relationship Some 1
A rare genetic cerebral small vessel disease characterized by an adult-onset primary microangiopathy with severe atherosclerosis of arterioles and secondary leukoencephalopathy. Patients may present with migraine, transient ischemic attacks, stroke with central facial palsy, cognitive dysfunction with impaired concentration, dementia, depression, movement disorder, vertigo, dysphagia, dysarthria, sicca syndrome, impaired REM sleep, and therapy-resistant hypertension, among others. Brain MRI typically shows a leukoencephalopathy that is disproportionately severe and extensive compared to the clinical disease. Finding site True Structure of capillary blood vessel Inferred relationship Some 2
Capillaroscopy Procedure site - Direct (attribute) True Structure of capillary blood vessel Inferred relationship Some 1
A life-threatening, rapidly progressive thrombotic disorder affecting mainly neonates and children that is characterized by purpuric skin lesions and disseminated intravascular coagulation. It may progress rapidly to multi-organ failure caused by thrombotic occlusion of small and medium-sized blood vessels. There are two forms of the disorder that are classified according to triggering mechanisms: acute infectious (the most common form), and idiopathic purpura fulminans. Finding site True Structure of capillary blood vessel Inferred relationship Some 2
Autoimmune thrombotic thrombocytopenic purpura (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 10
Acquired thrombotic thrombocytopenic purpura (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 10
Upshaw-Schulman syndrome (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 10
A rare renal disease characterized by thrombotic microangiopathy developing de novo in kidney transplant recipients with no evidence of occurrence of the disease prior to transplantation. Precipitating factors include antibody-mediated rejection, immunosuppressive medication, viral infections, and genetic abnormalities in the complement cascade, among others. The condition most commonly occurs within the first 3-6 months post-transplantation. Clinical presentation is highly variable and ranges from a limited form confined to the kidney with relatively good prognosis to a systemic variant consisting of the classic triad of thrombocytopenia, microangiopathic hemolytic anemia, and acute kidney injury. Finding site True Structure of capillary blood vessel Inferred relationship Some 1
A rare vascular anomaly characterized by the association of capillary and venous malformations with hypotrophy or shortening of an affected limb due to alterations in bones, muscles, or subcutaneous tissues. In most cases, at least one of the findings is noted shortly after birth, while the other components become evident later in infancy. Finding site True Structure of capillary blood vessel Inferred relationship Some 2
Thrombotic microangiopathy following hemopoietic stem cell transplant (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Infantile haemangioma of liver Finding site True Structure of capillary blood vessel Inferred relationship Some 2
Giant infantile haemangioma Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Infantile hemangioma of subglottis (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 2
Segmental infantile hemangioma Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Infantile hemangioma (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 1
Structure of capillary blood vessel of orbital region (body structure) Is a True Structure of capillary blood vessel Inferred relationship Some
Hemolytic uremic syndrome, adult type Finding site True Structure of capillary blood vessel Inferred relationship Some 11
Hemolytic uremic syndrome of childhood Finding site True Structure of capillary blood vessel Inferred relationship Some 12
Diarrhea-associated hemolytic uremic syndrome (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 13
Diarrhea-negative hemolytic uremic syndrome (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 11
Atypical haemolytic uraemic syndrome Finding site True Structure of capillary blood vessel Inferred relationship Some 12
Congenital hemolytic uremic syndrome (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 11
Hemolytic uremic syndrome Finding site True Structure of capillary blood vessel Inferred relationship Some 10
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. Finding site True Structure of capillary blood vessel Inferred relationship Some 2
A rare genetic hemolytic uremic syndrome (HUS) characterized by infantile onset of relapsing episodes of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. The episodes are often preceded by viral infections. Affected individuals typically present persistent hypertension, hematuria, and proteinuria (sometimes in the nephrotic range) and develop chronic kidney disease with age. Finding site True Structure of capillary blood vessel Inferred relationship Some 11
A rare type of hemolytic uremic syndrome (HUS) characterized by the triad of hemolytic anemia due to generalized thrombotic microangiopathy, thrombocytopenia, and acute kidney injury, and most commonly occurring after acute gastroenteritis due to Shiga toxin-producing enterohemorrhagic Escherichia coli or Shigella dysenteriae. Other infectious causes of HUS include Streptococcus pneumoniae, HIV, Mycoplasma pneumoniae, Histoplasmosis, and Coxsackie virus. Finding site True Structure of capillary blood vessel Inferred relationship Some 12
Atypical haemolytic uraemic syndrome with complement gene abnormality Finding site True Structure of capillary blood vessel Inferred relationship Some 14
Atypical haemolytic uraemic syndrome with anti-factor H antibodies Finding site True Structure of capillary blood vessel Inferred relationship Some 13
Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 2
Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect, aortic coarctation, eye abnormality, sternal anomalies syndrome (disorder) Finding site True Structure of capillary blood vessel Inferred relationship Some 3

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Reference Sets

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

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