Preferred Name

Severe combined immunodeficiency

ID

http://www.orpha.net/ORDO/Orphanet_183660

alternative_term

SCID

definition

Severe combined immunodeficiency (SCID) comprises a group of rare monogenic primary immunodeficiency disorders characterized by a lack of functional peripheral T lymphocytes resulting in early-onset severe respiratory infections and failure to thrive. They are classified according to immunological phenotype into SCID with absence of T cells but presence of B cells (T-B+ SCID) or SCID with absence of both (T-B- SCID) (see these terms). Both of these groups include several forms, with or without natural killer (NK) cells.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=183660

has_age_of_onset

Neonatal

Infancy

has_inheritance

X-linked recessive

Autosomal recessive

hasDbXref

MeSH:D016511

MedDRA:10069566

UMLS:C0085110

ICD-11:4A01.10

label

Severe combined immunodeficiency

notation

ORPHA:183660

Clinical group

prefixIRI

ORDO:Orphanet_183660

prefLabel

Severe combined immunodeficiency

present_in

Greece AND has_birth_prevalence_average_value : 1.7 AND has_birth_prevalence_range : 1-9 / 100 000

Worldwide AND has_point_prevalence_range : Unknown

France AND has_birth_prevalence_average_value : 1.6 AND has_birth_prevalence_range : 1-9 / 100 000

United States AND has_birth_prevalence_average_value : 1.72 AND has_birth_prevalence_range : 1-9 / 100 000

Costa rica AND has_birth_prevalence_average_value : 3.79 AND has_birth_prevalence_range : 1-9 / 100 000

Worldwide AND has_birth_prevalence_range : 1-9 / 100 000

Australia AND has_birth_prevalence_average_value : 1.75 AND has_birth_prevalence_range : 1-9 / 100 000

Chile AND has_birth_prevalence_average_value : 1.28 AND has_birth_prevalence_range : 1-9 / 100 000

Europe AND has_birth_prevalence_average_value : 1.65 AND has_birth_prevalence_range : 1-9 / 100 000

subClassOf

http://www.orpha.net/ORDO/Orphanet_101972

http://www.orpha.net/ORDO/Orphanet_506219

http://www.orpha.net/ORDO/Orphanet_557492

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http://purl.obolibrary.org/obo/HP_0004430 Coronavirus Infectious Disease Ontology / 冠状病毒感染性疾病本体 LOOM
http://purl.obolibrary.org/obo/HP_0004430 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.bioontology.org/ontology/LNC/LA12566-8 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3472 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.obolibrary.org/obo/MONDO_0015974 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0015974 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/LNC/LP111254-1 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://purl.bioontology.org/ontology/MESH/D016511 Medical Subject Headings / 医学主题词表 LOOM
http://purl.bioontology.org/ontology/LNC/MTHU036640 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://purl.obolibrary.org/obo/DOID_627 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_627 Human Disease Ontology / 人类疾病本体 LOOM
http://www.orpha.net/ORDO/Orphanet_183660 Experimental Factor Ontology / 实验性因素本体 SAME_URI
http://purl.bioontology.org/ontology/OMIM/MTHU009056 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM