30630007: Neutrophil count (procedure)

SNOMED CT Concept\Procedure\Procedure by method\Determination of a value, conclusion, or inference by evaluating evidence\An observation, by some objective method, of amount, number, quantity, size, level, extent, or magnitude, resulting in an ordinal or quantitative value\Cell count\Blood cell count\White blood cell count\Granulocyte count (procedure)\Neutrophil count

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

51268016 Neutrophil count en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

761655014 Neutrophil count (procedure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Neutrophil count	Is a	Blood cell count	false	Inferred relationship	Some
Neutrophil count	Method	Investigation - action	false	Inferred relationship	Some
Neutrophil count	Has measured component (attribute)	Blood cell	false	Inferred relationship	Some
Neutrophil count	Has measured component (attribute)	Neutrophilic granulocytic cell	false	Inferred relationship	Some
Neutrophil count	Has intent	Diagnostic intent (qualifier value)	false	Inferred relationship	Some
Neutrophil count	Is a	White blood cell test	false	Inferred relationship	Some
Neutrophil count	Component	Hematology observable	false	Inferred relationship	Some
Neutrophil count	Has specimen	White blood cell specimen (specimen)	false	Inferred relationship	Some
Neutrophil count	Component	Leukocyte	false	Inferred relationship	Some	2
Neutrophil count	Method	Evaluation - action	false	Inferred relationship	Some
Neutrophil count	Method	Measurement - action	false	Inferred relationship	Some	2
Neutrophil count	Is a	White blood cell count	false	Inferred relationship	Some
Neutrophil count	Component	Neutrophilic granulocytic cell	true	Inferred relationship	Some	1
Neutrophil count	Is a	Granulocyte count (procedure)	true	Inferred relationship	Some
Neutrophil count	Method	Measurement - action	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Segmented neutrophil count, blood	Is a	True	Neutrophil count	Inferred relationship	Some
Hypersegmented neutrophil count, blood	Is a	True	Neutrophil count	Inferred relationship	Some
Neutrophil percent differential count	Is a	True	Neutrophil count	Inferred relationship	Some
Neutrophil band count	Is a	True	Neutrophil count	Inferred relationship	Some
Neutrophil count NOS	Is a	False	Neutrophil count	Inferred relationship	Some
Neutrophil count outside reference range	Interprets	False	Neutrophil count	Inferred relationship	Some	1
Neutropenia	Interprets	False	Neutrophil count	Inferred relationship	Some	1
Neutrophilia	Interprets	False	Neutrophil count	Inferred relationship	Some	1
Neutrophil count within reference range	Interprets	False	Neutrophil count	Inferred relationship	Some	1
Neutrophil count outside reference range	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Neutrophilia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Neutrophil count within reference range	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Transient neonatal neutropenia due to congenital viral infection	Interprets	True	Neutrophil count	Inferred relationship	Some	4
Transient neonatal neutropenia due to neonatal bacterial sepsis (disorder)	Interprets	True	Neutrophil count	Inferred relationship	Some	4
Constitutional neutropenia	Interprets	False	Neutrophil count	Inferred relationship	Some	1
Acquired neutropenia	Interprets	False	Neutrophil count	Inferred relationship	Some	1
Non dose-related drug-induced neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Alloimmune neonatal neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Myelokathexis	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Toxic neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Neutropenia with dysgranulopoiesis	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Neutropenia associated with infectious disease	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Drug-induced neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Transient neonatal neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Dose-related drug-induced neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Immune neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Isoimmune neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Maternal transfer neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Shwachman syndrome	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Congenital neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Reticular dysgenesis	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Neutropenia associated with autoimmune disease	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Chronic benign neutropenia of childhood	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Chronic idiopathic immunoneutropenia in adult (disorder)	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Chronic hypoplastic neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Severe combined immunodeficiency with reticular dysgenesis (disorder)	Interprets	True	Neutrophil count	Inferred relationship	Some	3
Primary splenic neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Acquired neutropenia in newborn	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Cyclical neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
X-linked hypogammaglobulinemia	Interprets	False	Neutrophil count	Inferred relationship	Some	1
Chronic benign neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Metabolic neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Autoimmune neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Chronic familial neutropaenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Familial neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Chronic idiopathic neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Radiation agranulocytosis	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Neutropenia of the small for gestational age baby	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Chloramphenicol-induced neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Neutropenic disorder	Interprets	True	Neutrophil count	Inferred relationship	Some	1
De Vaal's syndrome (disorder)	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Reticular dysgenesis with congenital aleucocytosis	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Febrile neutropenia (disorder)	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Neutropenia with acquired immunodeficiency syndrome (disorder)	Interprets	True	Neutrophil count	Inferred relationship	Some	1
neutropénie provoquée par une chimiothérapie	Interprets	False	Neutrophil count	Inferred relationship	Some	1
Periodontitis co-occurrent with infantile genetic agranulocytosis	Interprets	False	Neutrophil count	Inferred relationship	Some	1
Periodontitis co-occurrent with acquired neutropenia	Interprets	False	Neutrophil count	Inferred relationship	Some	1
Periodontitis co-occurrent with familial neutropenia	Interprets	False	Neutrophil count	Inferred relationship	Some	1
Periodontitis co-occurrent with cyclical neutropenia	Interprets	False	Neutrophil count	Inferred relationship	Some	1
X-linked severe congenital neutropenia is an immunodeficiency syndrome characterized by recurrent major bacterial infections, severe congenital neutropenia, and monocytopenia. It has been described in five males spanning three generations of one family. It is transmitted as an X-linked recessive trait and is caused by mutations in the WAS gene, encoding the WASP protein.	Interprets	True	Neutrophil count	Inferred relationship	Some	1
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by moderate intellectual disability, dysmorphic facial features (such as prominent glabella, synophrys, and prognathism), generalized hirsutism, bilateral single palmar creases, and seizures. Additional reported manifestations include slowly progressive neurological deterioration with muscular weakness and impaired gait and balance, as well as hypogammaglobulinemia with specific absence of plasma and/or secretory IgA, among others. Brain imaging may show mild cerebellar atrophy and thin corpus callosum.	Interprets	False	Neutrophil count	Inferred relationship	Some	1
Neutropenia-monocytopenia-deafness syndrome is characterized by neutropenia with myeloid marrow hypoplasia, monocytopenia, and congenital deafness. It has been described in three siblings who suffered recurrent bacterial infections.	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Constitutional neutrophilia (disorder)	Interprets	True	Neutrophil count	Inferred relationship	Some	3
Neutrophilia disorder (disorder)	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Sweet's disease caused by drug	Interprets	True	Neutrophil count	Inferred relationship	Some	3
Drug-induced neutrophilia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Sweet's disease following infection (disorder)	Interprets	True	Neutrophil count	Inferred relationship	Some	2
Chronic neutrophilia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Stress neutrophilia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Acute febrile neutrophilic dermatosis	Interprets	True	Neutrophil count	Inferred relationship	Some	2
Acquired neutrophilia (disorder)	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Hereditary neutrophilia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Neutrophilic leukemoid reaction	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Acute neutrophilia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Corticosteroid-induced neutrophilia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Neutropaenia due to and following chemotherapy	Interprets	True	Neutrophil count	Inferred relationship	Some	1
A rare primary immunodeficiency disorder characterized by autosomal dominant inheritance, absolute neutrophil counts below 0.5x10E9/L in the peripheral blood (on three separate occasions over a six month period), granulopoiesis maturation arrest at the promyelocyte/myelocyte stage and early-onset, severe, recurrent bacterial infections.	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Kostmann syndrome is a rare, severe, congenital neutropenia disorder characterized by a lack of mature neutrophils (absolute neutrophil counts less than 500 cells/mm3) associated with frequent, recurrent bacterial infections (e.g. otitis media, pneumonia, sinusitis, urinary tract infections, abscesses of skin and/or liver) and increased promyelocytes in the bone marrow. Periodontal disease, as well as neurological symptoms, such as cognitive impairment, severe neurodegeneration and epilepsy, have been reported in some patients.	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Poikiloderma with neutropenia is a rare, genetic hereditary poikiloderma disorder characterized by early-onset poikiloderma (which typically begins in the extremities, progresses centripetally and eventually involves the trunk, face and ears) associated with chronic neutropenia, recurrent infections, pachyonychia and palmoplantar keratoderma. Growth and/or developmental delay and hepato- and/or splenomegaly are additional reported features.	Interprets	True	Neutrophil count	Inferred relationship	Some	1
A rare, genetic, primary immunodeficiency disorder characterized by severe congenital neutropenia, bone marrow fibrosis and neutrophil dysfunction which is refractory to granulocyte colony-stimulating factor, manifesting with life-threatening infections and/or deep-seated abscesses, hepato-/splenomegaly, thrombocytopenia, hypergammaglobulinemia, anemia with reticulocytosis and nephromegaly. Other reported features include osteosclerosis and neurological abnormalities (e.g. developmental delay, cortical blindness, hearing loss, thin corpus callosum or dysrhythmia on EEG).	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency is a rare, genetic, primary immunodeficiency disorder characterized by increased susceptibility to recurrent, life-threatening bacterial infections, in association with typically severe neutropenia in peripheral blood and bone marrow and a prominent ectatic superficial vein pattern, resulting from recessively inherited mutations in the G6PC3 gene. Cardiac malformations (e.g. atrial septal defects, patent ductus arteriosus, valvular defects), urogenital anomalies (including cryptorchidism), growth and developmental delay, facial dysmorphism (e.g. frontal bossing, upturned nose, malar hypoplasia), and intermittent thrombocytopenia are frequently associated.	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Pyoderma gangrenosum (disorder)	Interprets	False	Neutrophil count	Inferred relationship	Some	3
A rare, genetic, primary immunodeficiency disorder characterized by predisposition to recurrent, life-threatening bacterial infections associated with decreased peripheral neutrophil granulocytes (absolute neutrophil count less than 500 cells/microliter), resulting from recessively inherited loss-of-function mutations in the CSF3R gene. Full maturation of all three lineages in the bone marrow and refractoriness to in vivo rhG-CSF treatment are associated.	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency is a rare, genetic, primary immunodeficiency disorder characterized by early-onset, recurrent, severe bacterial infections, granulopoiesis maturation arrest at the promyelocyte/myelocyte stage and markedly reduced absolute neutrophil counts, resulting from recessively inherited mutations in the JAGN1 gene. Mild facial dysmorphism (i.e. triangular face), short stature, failure to thrive, hypothyroidism, developmental delay, pancreatic insufficiency and coarctation of aorta, as well as bone and urogenital abnormalities, may also be associated.	Interprets	True	Neutrophil count	Inferred relationship	Some	1
A rare, genetic, primary immunodeficiency disorder characterized by recurrent bacterial infections (including septic thrombophlebitis and subacute bacterial endocarditis) and neutropenia without lymphopenia or warts, resulting from recessively inherited mutations in CXCR2.	Interprets	True	Neutrophil count	Inferred relationship	Some	1
A rare, acquired immunodeficiency disease characterized by adult-onset absolute neutrophil counts less than 1.5 x 10^9/L on at least 3 occasions in a 3 month period that cannot be attributable to drugs or a specific genetic, infectious, inflammatory, autoimmune or malignant cause. Recurrent apthous stomatitis and a history of mild bacterial infections are typically associated. A benign outcome with a low rate of severe infections and no secondary malignancies is observed.	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Neutropenic sepsis (disorder)	Interprets	True	Neutrophil count	Inferred relationship	Some	2
Pyogenic arthritis-pyoderma gangrenosum-acne syndrome is a rare pleiotropic autoinflammatory disorder of childhood, primarily affecting the joints and skin.	Interprets	False	Neutrophil count	Inferred relationship	Some	4
Neutrophilic dermatosis (disorder)	Interprets	False	Neutrophil count	Inferred relationship	Some	3
Parastomal pyoderma gangrenosum (disorder)	Interprets	False	Neutrophil count	Inferred relationship	Some	3
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia is a rare, genetic, constitutional dyserythropoietic anemia disorder characterized by moderate to severe anemia without thrombocytopenia, variable degrees of neutropenia, and bone marrow biopsy findings of trilineage dysplasia and hypocellularity of erythroid and granulocytic lineages. Peripheral blood findings include anisocytosis, macrocytosis, poikilocytosis, elliptocytes, and fragmented erythrocytes.	Interprets	True	Neutrophil count	Inferred relationship	Some	3
A rare skin disease belonging to the spectrum of autoinflammatory syndromes characterized by the triad of pyoderma gangrenosum (PG), suppurative hidradenitis (SH) and acne.	Interprets	True	Neutrophil count	Inferred relationship	Some	4
Bullous pyoderma gangrenosum	Interprets	False	Neutrophil count	Inferred relationship	Some	4
Onycho-tricho-dysplasia neutropenia syndrome	Interprets	True	Neutrophil count	Inferred relationship	Some	3
Bowel-associated dermatosis-arthritis syndrome	Interprets	False	Neutrophil count	Inferred relationship	Some	2
syndrome post bypass intestinal	Interprets	False	Neutrophil count	Inferred relationship	Some	3
Benign ethnic neutropenia (disorder)	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Acquired neutropenia	Interprets	True	Neutrophil count	Inferred relationship	Some	1
Neutrophilic eccrine hidradenitis	Interprets	False	Neutrophil count	Inferred relationship	Some	4
Neutrophilic eccrine hidradenitis due to cytotoxic therapy (disorder)	Interprets	True	Neutrophil count	Inferred relationship	Some	1

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Id	Description	Lang	Type	Status	Case?	Module
51268016	Neutrophil count	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
761655014	Neutrophil count (procedure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core