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37548006: Hypopigmentation-immunodeficiency disease (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
62635016 Hypopigmentation-immunodeficiency disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
213742016 Griscelli syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
486742016 Chediak-Higashi-like syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
486743014 Griscelli syndrome with immunodeficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
486744015 Partial albinism with immunodeficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769427015 Hypopigmentation-immunodeficiency disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
62635016 Hypopigmentation-immunodeficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
62635016 Hypopigmentation-immunodeficiency disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
62636015 Giscelli syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
213742016 Griscelli syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
486742016 Chediak-Higashi-like syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
486743014 Griscelli syndrome with immunodeficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
486744015 Partial albinism with immunodeficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
486744015 Partial albinism with immunodeficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769427015 Hypopigmentation-immunodeficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
769427015 Hypopigmentation-immunodeficiency disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3412161001000113 Griscelli-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6280101000241110 syndrome d'immunodéficience et hypopigmentation fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6280111000241112 syndrome d'albinisme partiel et déficit immunitaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6280121000241117 syndrome de Griscelli fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6280101000241110 syndrome d'immunodéficience et hypopigmentation fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6280111000241112 syndrome d'albinisme partiel et déficit immunitaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6280121000241117 syndrome de Griscelli fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3412161001000113 Griscelli-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypopigmentation-immunodeficiency disease Is a Albinism false Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Is a Hereditary disorder of immune system false Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Is a Immunodeficiency associated with multiple organ system abnormalities true Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Is a Congenital immunodeficiency disease true Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Finding site Structure of immune system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypopigmentation-immunodeficiency disease Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypopigmentation-immunodeficiency disease Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypopigmentation-immunodeficiency disease Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypopigmentation-immunodeficiency disease Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypopigmentation-immunodeficiency disease Finding site Eye region structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypopigmentation-immunodeficiency disease Is a Site-specific disorder of skin false Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Is a Hereditary disorder of the integument (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Is a Disorder of tyrosine metabolism (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Is a Congenital deficiency of pigment of skin false Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypopigmentation-immunodeficiency disease Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypopigmentation-immunodeficiency disease Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypopigmentation-immunodeficiency disease Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypopigmentation-immunodeficiency disease Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypopigmentation-immunodeficiency disease Pathological process (attribute) Abnormal immune process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypopigmentation-immunodeficiency disease Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypopigmentation-immunodeficiency disease Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypopigmentation-immunodeficiency disease Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypopigmentation-immunodeficiency disease Is a Congenital malformation true Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Is a Disorder of pigmentation (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Hypopigmentation-immunodeficiency disease type 1 (disorder) Is a True Hypopigmentation-immunodeficiency disease Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease type 3 (disorder) Is a True Hypopigmentation-immunodeficiency disease Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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