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36070007: Wiskott-Aldrich 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
60191017 Wiskott-Aldrich syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
60193019 Immunodeficiency with thrombocytopenia AND eczema en Synonym Active Only initial character case insensitive SNOMED CT core module
767779011 Wiskott-Aldrich syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1228350017 Eczema, thrombocytopenia, immunodeficiency syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
1228351018 WAS - Wiskott-Aldrich syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
1228352013 Aldrich syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3036167017 Wiskott Aldrich syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Wiskott-Aldrich syndrome Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Is a Dense body defect true Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Is a Immunodeficiency associated with multiple organ system abnormalities true Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Is a Hereditary disorder of immune system true Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Is a Congenital anomaly of the hematopoietic system false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Is a Eczema false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Is a Congenital immunodeficiency disease true Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Is a Thrombocytopenia false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Associated morphology Papulovesicular rash false Inferred relationship Existential restriction modifier 1
Wiskott-Aldrich syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Wiskott-Aldrich syndrome Finding site Structure of immune system true Inferred relationship Existential restriction modifier 5
Wiskott-Aldrich syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Wiskott-Aldrich syndrome Finding site Platelet false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Is a Congenital thrombocytopenia false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Associated morphology Inflammation false Inferred relationship Existential restriction modifier 1
Wiskott-Aldrich syndrome Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Wiskott-Aldrich syndrome Has definitional manifestation Platelet count below reference range false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Wiskott-Aldrich syndrome Associated morphology Inflammation false Inferred relationship Existential restriction modifier 1
Wiskott-Aldrich syndrome Is a Hereditary thrombocytopenic disorder true Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Is a Hereditary disorder of cellular element of blood false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Has definitional manifestation Platelet count below reference range false Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Is a Hereditary cancer-predisposing syndrome true Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 1
Wiskott-Aldrich syndrome Interprets Platelet count true Inferred relationship Existential restriction modifier 1
Wiskott-Aldrich syndrome Is a Congenital thrombocytopenia true Inferred relationship Existential restriction modifier
Wiskott-Aldrich syndrome Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 4
Wiskott-Aldrich syndrome Has interpretation Abnormal false Inferred relationship Existential restriction modifier 3
Wiskott-Aldrich syndrome Interprets Hemostatic function true Inferred relationship Existential restriction modifier 3
Wiskott-Aldrich syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier 3
Wiskott-Aldrich syndrome Is a Immune thrombocytopenia true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Wiskott-Aldrich autosomal dominant variant syndrome Is a True Wiskott-Aldrich syndrome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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