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37548006: Hypopigmentation-immunodeficiency disease (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
62635016 Hypopigmentation-immunodeficiency disease en Synonym Active Entire term case insensitive SNOMED CT core module
62636015 Giscelli syndrome en Synonym Inactive Entire term case sensitive SNOMED CT core module
213742016 Griscelli syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
486742016 Chediak-Higashi-like syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
486743014 Griscelli syndrome with immunodeficiency en Synonym Active Entire term case sensitive SNOMED CT core module
486744015 Partial albinism with immunodeficiency en Synonym Active Entire term case insensitive SNOMED CT core module
769427015 Hypopigmentation-immunodeficiency disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core 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
Hypopigmentation-immunodeficiency disease Is a Hereditary disorder of immune system false Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Is a Immunodeficiency associated with multiple organ system abnormalities true Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Is a Congenital immunodeficiency disease true Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Finding site Structure of immune system true Inferred relationship Existential restriction modifier 2
Hypopigmentation-immunodeficiency disease Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 3
Hypopigmentation-immunodeficiency disease Occurrence Congenital false Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Finding site Structure of skin region false Inferred relationship Existential restriction modifier 2
Hypopigmentation-immunodeficiency disease Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Hypopigmentation-immunodeficiency disease Finding site Structure of eye proper false Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier 1
Hypopigmentation-immunodeficiency disease Finding site Eye region structure false Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 3
Hypopigmentation-immunodeficiency disease Is a Site-specific disorder of skin false Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Is a Disorder of tyrosine metabolism true Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Is a Congenital deficiency of pigment of skin false Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Hypopigmentation-immunodeficiency disease Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Hypopigmentation-immunodeficiency disease Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Hypopigmentation-immunodeficiency disease Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 2
Hypopigmentation-immunodeficiency disease Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
Hypopigmentation-immunodeficiency disease Pathological process Abnormal immune process false Inferred relationship Existential restriction modifier 1
Hypopigmentation-immunodeficiency disease Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier 3
Hypopigmentation-immunodeficiency disease Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Hypopigmentation-immunodeficiency disease Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Hypopigmentation-immunodeficiency disease Is a Congenital malformation true Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Is a Disorder of pigmentation true Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Hypopigmentation-immunodeficiency disease type 1 Is a True Hypopigmentation-immunodeficiency disease Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease type 3 Is a True Hypopigmentation-immunodeficiency disease Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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