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77121009: X-linked lymphoproliferative syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
128034012 X-linked lymphoproliferative syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
817917012 X-linked lymphoproliferative syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1234060015 XLPS - X-linked lymphoproliferative syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
1234062011 Duncan's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
4008251015 Purtilo syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
4636988011 Familial fatal Epstein-Barr infection en Synonym Active Only initial character case insensitive SNOMED CT core module
4636989015 Severe susceptibility to Epstein-Barr infection en Synonym Active Only initial character case insensitive SNOMED CT core module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked lymphoproliferative syndrome Is a Hereditary disorder of lymphatic system false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Is a Hereditary disorder of hematologic system false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Is a Hereditary disorder of immune system true Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Is a Immunodeficiency with major anomalies false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Is a Congenital immunodeficiency disease false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Is a Congenital anomaly of the hematopoietic system false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Is a Atypical lymphoproliferative disorder true Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Associated morphology Immunoproliferative morphology false Inferred relationship Existential restriction modifier 2
X-linked lymphoproliferative syndrome Pathological process Malignant neoplastic process false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Finding site Lymphoid system structure false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Finding site Leukocyte false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Associated morphology Malignant neoplasm of primary, secondary, or uncertain origin false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Pathological process Neoplastic process false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
X-linked lymphoproliferative syndrome Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Finding site Lymphocytic tissue structure false Inferred relationship Existential restriction modifier 1
X-linked lymphoproliferative syndrome Associated morphology Proliferation false Inferred relationship Existential restriction modifier 1
X-linked lymphoproliferative syndrome Finding site Structure of immune system false Inferred relationship Existential restriction modifier 2
X-linked lymphoproliferative syndrome Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Associated morphology White blood cell abnormality false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Finding site Structure of immune system false Inferred relationship Existential restriction modifier 3
X-linked lymphoproliferative syndrome Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Associated morphology Lymphoproliferative disorder true Inferred relationship Existential restriction modifier 1
X-linked lymphoproliferative syndrome Pathological process Abnormal immune process false Inferred relationship Existential restriction modifier 4
X-linked lymphoproliferative syndrome Is a Disorder of immune structure true Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Is a Primary immune deficiency disorder true Inferred relationship Existential restriction modifier
X-linked lymphoproliferative syndrome Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 1
X-linked lymphoproliferative syndrome Finding site Structure of immune system true Inferred relationship Existential restriction modifier 1
X-linked lymphoproliferative syndrome Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Fatal infectious mononucleosis associated with X-linked lymphoproliferative syndrome Associated with False X-linked lymphoproliferative syndrome Inferred relationship Existential restriction modifier 2
X-linked lymphoproliferative disease due to SH2D1A deficiency Is a True X-linked lymphoproliferative syndrome Inferred relationship Existential restriction modifier
X-linked lymphoproliferative disease due to XIAP deficiency Is a True X-linked lymphoproliferative syndrome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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