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37548006: Hypopigmentation-immunodeficiency disease (disorder)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
213742016 Griscelli syndrome en Synonym Active Case sensitive SNOMED CT core
486742016 Chediak-Higashi-like syndrome en Synonym Active Case sensitive SNOMED CT core
486743014 Griscelli syndrome with immunodeficiency en Synonym Active Case sensitive SNOMED CT core
486744015 Partial albinism with immunodeficiency en Synonym Active Case insensitive SNOMED CT core
62635016 Hypopigmentation-immunodeficiency disease en Synonym Active Case insensitive SNOMED CT core
62636015 Giscelli syndrome en Synonym Inactive Case sensitive SNOMED CT core
769427015 Hypopigmentation-immunodeficiency disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core

2 descendants. Search Descendants:

Expanded Value Set

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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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