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414030009: Disorder of immune structure (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
2530846019 Disorder of immune structure (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2534310012 Disorder of immune structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6073981000241110 affection d'une structure immunitaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6073991000241112 affection d'une structure du système immunitaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1345 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Disorder of immune structure (disorder) Is a Disorder of body system true Inferred relationship Some
Disorder of immune structure (disorder) Finding site Structure of immune system (body structure) true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Combined immunodeficiency due to OX40 deficiency is a rare, combined T and B cell immunodeficiency characterised by susceptibility to develop an aggressive, childhood-onset, disseminated, cutaneous and systemic Kaposi sarcoma. Is a True Disorder of immune structure (disorder) Inferred relationship Some
Hennekam lymphangiectasia-lymphedema syndrome (disorder) Is a True Disorder of immune structure (disorder) Inferred relationship Some
Mast cell disorder (disorder) Is a True Disorder of immune structure (disorder) Inferred relationship Some
Autoimmune lymphoproliferative syndrome Is a True Disorder of immune structure (disorder) Inferred relationship Some
Deficiency of immunoglobulin A with immunoglobulin G subclass deficiency (disorder) Is a True Disorder of immune structure (disorder) Inferred relationship Some
Disorder of eosinophil (disorder) Is a True Disorder of immune structure (disorder) Inferred relationship Some
Lymphocytic hypoplasia Is a True Disorder of immune structure (disorder) Inferred relationship Some
X-linked lymphoproliferative syndrome Is a True Disorder of immune structure (disorder) Inferred relationship Some
Immunoglobulin G deficiency due to multiple myeloma Is a True Disorder of immune structure (disorder) Inferred relationship Some
Immunoglobulin G deficiency due to monoclonal gammopathy of undetermined significance (disorder) Is a True Disorder of immune structure (disorder) Inferred relationship Some
B cell lymphocyte aplasia caused by drug (disorder) Is a True Disorder of immune structure (disorder) Inferred relationship Some
X-linked immunoneurologic disorder is characterized by immune deficiency and neurological disorders in females, and by neonatal death in males. Is a True Disorder of immune structure (disorder) Inferred relationship Some
Functional disorder of polymorphonuclear neutrophil (disorder) Is a True Disorder of immune structure (disorder) Inferred relationship Some
Immune effector cell-associated neurotoxicity syndrome (disorder) Is a True Disorder of immune structure (disorder) Inferred relationship Some
Cytokine-associated toxicity (disorder) Is a True Disorder of immune structure (disorder) Inferred relationship Some
A rare, genetic, developmental defect during embryogenesis malformation syndrome characterized by severe postnatal growth retardation, craniofacial dysmorphism, which includes a progeroid facial appearance, brachycephaly with hypoplasia of the frontal and parietal tubers and a flat occipital area, narrow forehead, prominent glabella, small orbit, slight bilateral exophthalmos, straight nose, hypoplastic cheekbones, long philtrum and thin lips, skeletal abnormalities (i.e. micromelia, brachydactyly, and severe short stature with short limbs), normal intelligence, Pelger-Huët anomaly of leukocytes, loose skin with decreased tissue turgor, and bilateral optic atrophy with loss of color vision and visual acuity. Recurrent liver failure triggered by fever has been occasionally reported. Radiographs may evidence delayed bone age, late ossification and/or osteoporosis. Is a True Disorder of immune structure (disorder) Inferred relationship Some
Common variable agammaglobulinemia Is a False Disorder of immune structure (disorder) Inferred relationship Some
Common variable immunodeficiency Is a True Disorder of immune structure (disorder) Inferred relationship Some
Atypical haemolytic uraemic syndrome with complement gene abnormality Is a True Disorder of immune structure (disorder) Inferred relationship Some
X-linked agammaglobulinemia Is a True Disorder of immune structure (disorder) Inferred relationship Some

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