FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

127068004: Histiocytic syndrome (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
356016 Histiocytic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
731110011 Histiocytic syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3035345016 Histiocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2081231000005118 Histiocytært syndrom da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

89 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Histiocytic syndrome Is a Disorder of immune system false Inferred relationship Some
Histiocytic syndrome Is a White blood cell disorder (disorder) false Inferred relationship Some
Histiocytic syndrome Finding site Haematopoietic system structure false Inferred relationship Some
Histiocytic syndrome Finding site Structure of immune system (body structure) false Inferred relationship Some
Histiocytic syndrome Finding site Leukocyte false Inferred relationship Some
Histiocytic syndrome Finding site Haematopoietic system structure false Inferred relationship Some
Histiocytic syndrome Associated morphology White blood cell abnormality false Inferred relationship Some
Histiocytic syndrome Is a Disorder of hematopoietic cell proliferation (disorder) true Inferred relationship Some
Histiocytic syndrome Associated morphology Histiocytær proliferation false Inferred relationship Some 1
Histiocytic syndrome Associated morphology Histiocytic proliferation (morphologic abnormality) true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
histiocytose X-syndrom Is a False Histiocytic syndrome Inferred relationship Some
Hemolytic erythrophagocytic syndrome Is a True Histiocytic syndrome Inferred relationship Some
Langerhan's cell histiocytosis Is a False Histiocytic syndrome Inferred relationship Some
Benign cephalic histiocytosis Is a True Histiocytic syndrome Inferred relationship Some
Hæmofagocytosesyndrom Is a False Histiocytic syndrome Inferred relationship Some
Malignant histiocytic disorder Is a False Histiocytic syndrome Inferred relationship Some
Rosai-Dorfman disease Is a False Histiocytic syndrome Inferred relationship Some
Sea-blue histiocyte syndrome Is a True Histiocytic syndrome Inferred relationship Some
Langerhans cell histiocytosis (disorder) Is a False Histiocytic syndrome Inferred relationship Some
Xanthogranuloma Is a True Histiocytic syndrome Inferred relationship Some
[X]Other histiocytosis syndromes Is a False Histiocytic syndrome Inferred relationship Some
Histiocytic and mast cell tumor of uncertain behavior Is a False Histiocytic syndrome Inferred relationship Some
Neoplasm of uncertain behavior of histiocytic and mast cells Is a False Histiocytic syndrome Inferred relationship Some
Xanthoma disseminatum (disorder) Is a True Histiocytic syndrome Inferred relationship Some
Juvenile xanthogranuloma (disorder) Is a False Histiocytic syndrome Inferred relationship Some
Multiple eruptive juvenile xanthogranuloma (disorder) Is a False Histiocytic syndrome Inferred relationship Some
Non-Langerhans cell histiocytic dermatosis (disorder) Is a True Histiocytic syndrome Inferred relationship Some
Mucinous histiocytosis of the colon Is a True Histiocytic syndrome Inferred relationship Some
Lipoid dermatoarthritis (disorder) Is a False Histiocytic syndrome Inferred relationship Some
Cytophagic histiocytic panniculitis Associated with True Histiocytic syndrome Inferred relationship Some 2
Panniculitis secondary to histiocytic disorder (disorder) Associated with True Histiocytic syndrome Inferred relationship Some 2
Erdheim-Chester disease Is a False Histiocytic syndrome Inferred relationship Some
Chronic histiocytosis Is a True Histiocytic syndrome Inferred relationship Some
History of histiocytosis (situation) Associated finding True Histiocytic syndrome Inferred relationship Some 1
Periodontitis due to histiocytosis syndrome (disorder) Due to True Histiocytic syndrome Inferred relationship Some 1
A rare cutaneous disease and a systemic inherited histiocytosis with main characteristics of hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, low height, and occasionally, hyperglycaemia/diabetes mellitus. The syndrome becomes clinically apparent mostly during childhood, but cases during infancy and late-onset cases have been reported too. Caused by mutations in SLC29A3 (10q22.2) (encoding a nucleoside transporter, hENT3), which result in defective nucleoside transport functions of hENT3. This leads to histiocytic infiltration of numerous organs. Transmission is autosomal recessive. Is a True Histiocytic syndrome Inferred relationship Some
Histiocytic neoplasm (disorder) Is a True Histiocytic syndrome Inferred relationship Some

This concept is not in any reference sets

Back to Start