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720520009: Attenuated Chédiak-Higashi syndrome (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
3321117015 Attenuated Chédiak-Higashi syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3321118013 Attenuated Chédiak-Higashi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3321119017 Atypical Chédiak-Higashi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5402391017 A very rare and atypical form of Chédiak-Higashi syndrome (CHS), a genetic disorder characterized by partial oculocutaneous albinism, severe immunodeficiency, mild bleeding, neurological dysfunction and lymphoproliferative disorder. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402392012 A very rare and atypical form of Chédiak-Higashi syndrome (CHS), a genetic disorder characterised by partial oculocutaneous albinism, severe immunodeficiency, mild bleeding, neurological dysfunction and lymphoproliferative disorder. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321117015 Attenuated Chédiak-Higashi syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3321118013 Attenuated Chédiak-Higashi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3321119017 Atypical Chédiak-Higashi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3321120011 A very rare and atypical form of Chédiak-Higashi syndrome, a genetic disorder with characteristics of partial oculocutaneous albinism, severe immunodeficiency, mild bleeding, neurological dysfunction and lymphoproliferative disorder. Missense mutations in the LYST lysosomal gene (1q42.1-q42.2) appear to cause this form of Chédiak-Higashi syndrome. Inherited in an autosomal recessive manner. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402391017 A very rare and atypical form of Chédiak-Higashi syndrome (CHS), a genetic disorder characterized by partial oculocutaneous albinism, severe immunodeficiency, mild bleeding, neurological dysfunction and lymphoproliferative disorder. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402392012 A very rare and atypical form of Chédiak-Higashi syndrome (CHS), a genetic disorder characterised by partial oculocutaneous albinism, severe immunodeficiency, mild bleeding, neurological dysfunction and lymphoproliferative disorder. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3415231001000115 Chédiak-Higashi-Syndrom, attenuiertes de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
916181000172114 syndrome de Chédiak-Higashi atténué fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
963321000172115 syndrome de Chédiak-Higashi atypique fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
916181000172114 syndrome de Chédiak-Higashi atténué fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
963321000172115 syndrome de Chédiak-Higashi atypique fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3415231001000115 Chédiak-Higashi-Syndrom, attenuiertes 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
Attenuated Chédiak-Higashi syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Attenuated Chédiak-Higashi syndrome (disorder) Is a Chédiak-Higashi syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Attenuated Chédiak-Higashi syndrome (disorder) Finding site Structure of immune system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Attenuated Chédiak-Higashi syndrome (disorder) Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier (core metadata concept)
Attenuated Chédiak-Higashi syndrome (disorder) Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier (core metadata concept) 4
Attenuated Chédiak-Higashi syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Attenuated Chédiak-Higashi syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
Attenuated Chédiak-Higashi syndrome (disorder) Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 4
Attenuated Chédiak-Higashi syndrome (disorder) Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 5
Attenuated Chédiak-Higashi syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Attenuated Chédiak-Higashi syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Attenuated Chédiak-Higashi syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Attenuated Chédiak-Higashi syndrome (disorder) Finding site Structure of immune system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Attenuated Chédiak-Higashi syndrome (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Attenuated Chédiak-Higashi syndrome (disorder) Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 2
Attenuated Chédiak-Higashi syndrome (disorder) Interprets Hemostatic function false Inferred relationship Existential restriction modifier (core metadata concept) 3
Attenuated Chédiak-Higashi syndrome (disorder) Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 3
Attenuated Chédiak-Higashi syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Attenuated Chédiak-Higashi syndrome (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 3
Attenuated Chédiak-Higashi syndrome (disorder) Interprets Hemostatic function 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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