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Leukocyte disorder

MedGen UID:: 7325
•Concept ID:: C0023510
•: Disease or Syndrome

Synonym:	Leukocyte disease
SNOMED CT:	WBC diseases (54097007); White blood cell disorder (54097007)

Monarch Initiative:	MONDO:0004805

Definition

A disease involving leukocytes. [from MONDO]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVLeukocyte disorder

Pathological Conditions, Signs and Symptoms
- Pathological process
  - Disease
    - Disorder by Site
      - Hematopoietic and Lymphoid System Disorder
        Hematologic disorder
        Leukocyte disorder
        Eosinophilia
        Eosinophilia myalgia syndrome
        Eosinophilic esophagitis
        Childhood eosinophilic esophagitis
        Esophagitis, eosinophilic, 1
        Esophagitis, eosinophilic, 2
        Eosinophilic granuloma
        Episodic eosinophilia
        Hypereosinophilia
        Hypereosinophilic syndrome
        Idiopathic hypereosinophilic syndrome
        Primary hypereosinophilic syndrome
        Pulmonary eosinophilia
        Secondary hypereosinophilic syndrome
        Kimura disease
        Skin epithelioid hemangioma
        Penile Epithelioid Hemangioma
        Infectious mononucleosis
        Leukocytosis
        Leukemoid reaction
        Leukemoid reaction of the newborn
        Lymphocytosis
        Increased B cell count
        Increased T cell count
        Leukopenia
        Agranulocytosis
        Congenital agranulocytosis
        Drug-induced agranulocytosis
        Neutropenic disorder
        Lymphopenia
        Idiopathic CD4-positive T-lymphocytopenia
        Wiskott-Aldrich syndrome
        Leukostasis
        Pelger-Huët anomaly
        Phagocyte bactericidal dysfunction
        Chronic granulomatous disease
        Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
        Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 1
        Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
        Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3
        Granulomatous disease, chronic, X-linked
        Chédiak-Higashi syndrome
        Aleutian disease
        Hyper-IgE syndrome
        CADINS disease
        Hyper-IgE recurrent infection syndrome 1, autosomal dominant
        Immunodeficiency 23
        Netherton syndrome
        Severe dermatitis-multiple allergies-metabolic wasting syndrome
        STAT3 Deficiency

Professional guidelines

PubMed

Diagnosis and Treatment of Myelodysplastic Syndromes: A Review.

Sekeres MA, Taylor J
JAMA 2022 Sep 6;328(9):872-880. doi: 10.1001/jama.2022.14578. PMID: 36066514

ACG Clinical Guideline: Management of Irritable Bowel Syndrome.

Lacy BE, Pimentel M, Brenner DM, Chey WD, Keefer LA, Long MD, Moshiree B
Am J Gastroenterol 2021 Jan 1;116(1):17-44. doi: 10.14309/ajg.0000000000001036. PMID: 33315591

ACG Clinical Guideline: Management of Crohn's Disease in Adults.

Lichtenstein GR, Loftus EV, Isaacs KL, Regueiro MD, Gerson LB, Sands BE
Am J Gastroenterol 2018 Apr;113(4):481-517. Epub 2018 Mar 27 doi: 10.1038/ajg.2018.27. PMID: 29610508

Supplemental Content

Table of contents

Clinical resources

ClinicalTrials.gov

Practice guidelines

PubMed
See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.
Bookshelf
See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

Consumer resources

MedlinePlus

Reviews

Related information

MeSH
Related Medical Subject Headings
PMC Articles
Related information in PubMed Central Links
PubMed
Related literature resources in PubMed

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Leukocyte disorder
Leukocyte disorder

MedGen
KRTAP19-8 keratin associated protein 19-8 [Homo sapiens]
KRTAP19-8 keratin associated protein 19-8 [Homo sapiens]
Gene ID:728299

Gene

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