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719827008: X-linked immunoneurologic disorder (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3318063019 X-linked immunoneurologic disorder (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3318064013 X-linked immunoneurologic disorder en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3318065014 Woods Black Norbury syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402241019 X-linked immunoneurologic disorder is characterized by immune deficiency and neurological disorders in females, and by neonatal death in males. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402242014 X-linked immunoneurologic disorder is characterised by immune deficiency and neurological disorders in females, and by neonatal death in males. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3318063019 X-linked immunoneurologic disorder (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3318064013 X-linked immunoneurologic disorder en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3318065014 Woods Black Norbury syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3318066010 A syndrome with characteristics of immune deficiency and neurological disorders in females and neonatal death in males. The syndrome has been described in only one family with nine affected individuals (five males and four females) spanning two generations. Symptomatic females present slowly progressive proximal muscle weakness, leg hyperreflexia, pes cavus, increased muscle tone in the legs, poor bladder function, static reduced night vision and frequent sinopulmonary infections associated with IgG2 deficiency. Males present with low birth weight and severe hypotonia that leads to death in the neonatal period. The gene locus has been mapped to Xq26-qter. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402241019 X-linked immunoneurologic disorder is characterized by immune deficiency and neurological disorders in females, and by neonatal death in males. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402242014 X-linked immunoneurologic disorder is characterised by immune deficiency and neurological disorders in females, and by neonatal death in males. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3443511001000117 Immuno-neurologische Krankheit, X-chromosomale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
904161000172112 syndrome de Woods-Black-Norbury fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1010751000172114 syndrome immuno-neurologique lié à l'X fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
904161000172112 syndrome de Woods-Black-Norbury fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1010751000172114 syndrome immuno-neurologique lié à l'X fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3443511001000117 Immuno-neurologische Krankheit, X-chromosomale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked immunoneurologic disorder Due to Chromosomal disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked immunoneurologic disorder Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
X-linked immunoneurologic disorder Is a Immunodeficiency associated with chromosomal abnormality false Inferred relationship Existential restriction modifier (core metadata concept)
X-linked immunoneurologic disorder Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier (core metadata concept)
X-linked immunoneurologic disorder Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked immunoneurologic disorder Is a X-linked dominant hereditary disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked immunoneurologic disorder Is a Primary immune deficiency disorder true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked immunoneurologic disorder Is a Hereditary disorder of immune system true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked immunoneurologic disorder Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked immunoneurologic disorder Is a Disorder of immune structure true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked immunoneurologic disorder Finding site Structure of immune system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked immunoneurologic disorder Finding site Nervous system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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